反応 #4171597
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-212aad6bd86a49b483b684bb224841c0表示可能な構造データがありません
CC(C)OC(=O)CCl製品情報
propan-2-yl 2-chloroacetate (CAS 105-48-6) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 7759
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-212aad6bd86a49b483b684bb224841c0反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-44af330e68aa4fbda9030f4243ca2d17反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 20 g of Co2 (CO)8 in 2.5 liters of isopropanol and 546 g (4 moles) of chloroacetic acid isopropyl ester are placed in a pressure vessel of a capacity of 18 liters, as in Example 1. At 55° C., and a pressure of 5 bars of CO, a 2.93% solution of sodium hydroxide in isopropanol is pumped into the vessel over a period of 3 hours, maintaining a pH of 7.0. At a transformation of 82%, 615 g of malonic acid diisopropyl ester (92% yield) is obtained after the usual processing. 98 g of chloroacetic acid isopropyl ester is recovered. maintaining a pH of 7.0
ソース ID: ord-ffe40bfa903a41ce950ae81b27983251反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-212aad6bd86a49b483b684bb224841c0反応条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 168 g of 2-thienylcarboxaldehyde and 12.9 g of isopropyl chloroacetate is then introduced over 30 minutes. The solution is stirred for 25 minutes at this temperature and 257 g of an aqueous solution of sodium hydroxide at a concentration of 35% are then added over 30 minutes. The mixture is stirred at 50° C. for 2 hours, is cooled to 25° C. and 161.5 g of hydroxylamine hydrochloride dissolved in 200 ml of water are then introduced over 30 minutes. The mixture is kept stirred for 30 minutes and is then added to 1.5 l of water and 1.5 l of dichloromethane. is then introduced over 30 minutes are then added over 30 minutes is cooled to 25° C. are then introduced over 30 minutes The mixture is kept stirred for 30 minutes
ソース ID: ord-2757e7a18a954c8396c2cb67dba87d3d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 35.7 g of isopropyl 2-chloroacetate is added to a suspension of 33.5 g of 4-phenylthiosemicarbazide in 150 ml of tetrahydrofuran. After the mixture has been stirred for 30 minutes it is boiled for a further 30 minutes and then allowed to cool. The precipitated solid is isolated by suction filtering, washed with acetone and the residue is heated in a water/acetone mixture (1:1). After the separated sulfur has been poured off, the whole is allowed to cool and is neutralized with aqueous NaHCO3, solution and the precipitated solid is isolated; m.p. 138°-139° C. (from toluene). is boiled for a further 30 minutes to cool The precipitated solid is isolated by suction filtering washed with acetone the residue is heated in a water/acetone mixture (1:1) After the separated sulfur has been poured off to cool the precipitated solid is isolated
ソース ID: ord-d16790c1377a4c428b0eea47a823bc70反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 35.7 g of isopropyl 2-chloroacetate is added to a suspension of 33.5 g of 4-phenylthiosemicarbazide in 150 ml of tetrahydrofuran. After the mixture has been stirred for 30 minutes it is boiled for a further 30 minutes and then allowed to cool. The precipitated solid is isolated by suction filtering, washed with acetone and the residue is heated in a water/acetone mixture (1:1). After the separated sulfur has been poured off, the whole is allowed to cool and is neutralized with aqueous NaHCO3, solution and the precipitated solid is isolated; m.p. 138°-139° C. (from toluene). is boiled for a further 30 minutes to cool The precipitated solid is isolated by suction filtering washed with acetone the residue is heated in a water/acetone mixture (1:1) After the separated sulfur has been poured off to cool the precipitated solid is isolated
ソース ID: ord-d16790c1377a4c428b0eea47a823bc70反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 20 g of Co2 (CO)8 in 2.5 liters of isopropanol and 546 g (4 moles) of chloroacetic acid isopropyl ester are placed in a pressure vessel of a capacity of 18 liters, as in Example 1. At 55° C., and a pressure of 5 bars of CO, a 2.93% solution of sodium hydroxide in isopropanol is pumped into the vessel over a period of 3 hours, maintaining a pH of 7.0. At a transformation of 82%, 615 g of malonic acid diisopropyl ester (92% yield) is obtained after the usual processing. 98 g of chloroacetic acid isopropyl ester is recovered. maintaining a pH of 7.0
ソース ID: ord-6ef41d616fd74555927a6e5c401d3ff3反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 20 g of Co2 (CO)8 in 2.5 liters of isopropanol and 546 g (4 moles) of chloroacetic acid isopropyl ester are placed in a pressure vessel of a capacity of 18 liters, as in Example 1. At 55° C., and a pressure of 5 bars of CO, a 2.93% solution of sodium hydroxide in isopropanol is pumped into the vessel over a period of 3 hours, maintaining a pH of 7.0. At a transformation of 82%, 615 g of malonic acid diisopropyl ester (92% yield) is obtained after the usual processing. 98 g of chloroacetic acid isopropyl ester is recovered. maintaining a pH of 7.0
ソース ID: ord-ffe40bfa903a41ce950ae81b27983251反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 20 g of Co2 (CO)8 in 2.5 liters of isopropanol and 546 g (4 moles) of chloroacetic acid isopropyl ester are placed in a pressure vessel of a capacity of 18 liters, as in Example 1. At 55° C., and a pressure of 5 bars of CO, a 2.93% solution of sodium hydroxide in isopropanol is pumped into the vessel over a period of 3 hours, maintaining a pH of 7.0. At a transformation of 82%, 615 g of malonic acid diisopropyl ester (92% yield) is obtained after the usual processing. 98 g of chloroacetic acid isopropyl ester is recovered. maintaining a pH of 7.0
ソース ID: ord-ffe40bfa903a41ce950ae81b27983251反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 35.7 g of isopropyl 2-chloroacetate is added to a suspension of 33.5 g of 4-phenylthiosemicarbazide in 150 ml of tetrahydrofuran. After the mixture has been stirred for 30 minutes it is boiled for a further 30 minutes and then allowed to cool. The precipitated solid is isolated by suction filtering, washed with acetone and the residue is heated in a water/acetone mixture (1:1). After the separated sulfur has been poured off, the whole is allowed to cool and is neutralised with aqueous NaHCO3, solution and the precipated solid is isolated; m.p. 138°-139° C. (from toluene). is boiled for a further 30 minutes to cool The precipitated solid is isolated by suction filtering washed with acetone the residue is heated in a water/acetone mixture (1:1) After the separated sulfur has been poured off to cool the precipated solid is isolated
ソース ID: ord-24e7f3635ed94ceeaee84c5b15b9e5b6反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A suspension of tert-butyl 5-(2-(3-hydroxyphenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate (120 mg, 0.26 mmol), isopropyl 2-chloroacetate (45 mL, 0.36 mmol), K2CO3 (125 μL, 0.24 mmol), in DMF (5 mL) stirred at RT for 2 h. Concentrated in vacuo to afford the crude tert-butyl 5-(2-(3-(2-isopropoxy-2-oxoethoxy)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate. (0.26 mmol) Concentrated in vacuo
ソース ID: ord-6f207ee295f0458e972152cb87e98315PubChem References
化合物の公開データベース記録に掲載された情報源です。
関連製品
12 related records
CAS 26404-20-6
CAS 515-84-4
CAS 126176-76-9
CAS 3674-10-0
CAS 535-13-7
CAS 3974-99-0
CAS 39061-59-1
CAS 542-58-5
CAS 541-88-8
CAS 107-59-5
CAS 105-39-5
CAS 623-60-9
