反応 #4011078
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-1479cf30e4054722b480c65d7395e4bf表示可能な構造データがありません
BrC1C=C(C(C)=C(C=1)Cl)Cl製品情報
5-BROMO-1,3-DICHLORO-2-METHYLBENZENE (CAS 204930-37-0) 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 641155
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
7 反応 · 7 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-1479cf30e4054722b480c65d7395e4bf反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-1479cf30e4054722b480c65d7395e4bf反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Heat a solution of 5-bromo-1,3-dichloro-2-methylbenzene (97 mg, 0.40 mmol), N-bromosuccinimide (76 mg, 0.425 mmol) and benzoyl peroxide (16 mg, 0.06 mmol) in CCl4 (5 mL) to reflux for 3 hours under N2. Cool the reaction to room temperature and concentrate to an orange residue. Purify the residue by silica gel chromatography eluting with hexanes to afford 112 mg (87%) of the product as white crystals. to reflux for 3 hours under N2 Cool the reaction to room temperature concentrate to an orange residue Purify the residue by silica gel chromatography eluting with hexanes
ソース ID: ord-56bc74df5037491aa0512ac34fab2992反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Suspend the 3,5-dichloro-4-methylaniline in 48% HBr (5 mL) and water (5 mL) and heat with a heat gun until the mixture is near the boiling point. Cool the slurry to room temperature and then cool to 0° C. with an ice/brine bath. Add a solution of sodium nitrite (109 mg, 1.58 mmol) in water (2 mL) dropwise. After the addition is complete, stir the reaction an additional 15 min in the cold bath. Add a solution of CuBr (1.08 g, 7.53 mmol) in 48% HBr (2 mL) and heat the rapidly stirring reaction to 50° C. for 1 hour. Cool the reaction to room temperature, dilute the reaction with ethyl acetate and discard the aqueous layer. Wash the organic layer with water and brine, dry with MgSO4, filter through celite and concentrate to an orange residue. Purify the residue by silica gel chromatography eluting with hexanes to afford 164 mg (45%) of the product as a yellow solid. heat with a heat gun until the mixture cool to 0° C. with an ice/brine bath After the addition the reaction an additional 15 min in the cold bath heat the rapidly stirring reaction to 50° C. for 1 hour Cool the reaction to room temperature dilute Wash the organic layer with water and brine dry with MgSO4 filter through celite concentrate to an orange residue Purify the residue by silica gel chromatography eluting with hexanes
ソース ID: ord-21e693eafa8a43cbb7892bcea51d876b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Heat to reflux a solution of 5-bromo-1,3-dichloro-2-methylbenzene (97 mg, 0.40 mmol), N-bromosuccinimide (76 mg, 0.425 mmol) and benzoyl peroxide (16 mg, 0.06 mmol) in CCl4 (5 mL) for 3 hours under N2. Cool the reaction to room temperature and concentrate to an orange residue. Purify the residue by silica gel chromatography eluting with hexanes to afford 112 mg (87%) of the product as white crystals. Heat Cool the reaction to room temperature concentrate to an orange residue Purify the residue by silica gel chromatography eluting with hexanes
ソース ID: ord-528fb59ffc1f47bb9b46305a8d127424反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Suspend 3,5-dichloro-4-methylaniline in 48% HBr (5 mL) and water (5 mL) and heat with a heat gun until the mixture is near the boiling point. Cool the slurry to room temperature and then cool to 0° C. with an ice/brine bath. Add dropwise a solution of sodium nitrite (109 mg, 1.58 mmol) in water (2 mL). After the addition is complete, stir the reaction an additional 15 min in the cold bath. Add a solution of CuBr (1.08 g, 7.53 mmol) in 48% HBr (2 mL) and heat the rapidly stirring reaction to 50° C. for 1 hour. Cool the reaction to room temperature, dilute with EtOAc and discard the aqueous layer. Wash the organic layer with water and brine, dry with MgSO4, filter through celite and concentrate to an orange residue. Purify the residue by silica gel chromatography eluting with hexanes to afford 164 mg (45%) of the product as a yellow solid. heat with a heat gun until the mixture cool to 0° C. with an ice/brine bath After the addition the reaction an additional 15 min in the cold bath heat the rapidly stirring reaction to 50° C. for 1 hour Cool the reaction to room temperature Wash the organic layer with water and brine dry with MgSO4 filter through celite concentrate to an orange residue Purify the residue by silica gel chromatography eluting with hexanes
ソース ID: ord-c159d6a41741433ebf97aa3d280c2207反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-1479cf30e4054722b480c65d7395e4bfPubChem References
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