反応 #4153751
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-b08797dbc1b1416db51be7c3593bd6f2表示可能な構造データがありません
CC(C)CCC(=O)O製品情報
4-methylpentanoic acid (CAS 646-07-1) 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 12587
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-b08797dbc1b1416db51be7c3593bd6f2反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-473296d1fc664c1c92554b740ad09cae反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-65797f26c2f643cb9bd9b56a98ba342f反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b43563937f414c6594fafe05a111dc99反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f9a590115b814f478845b3f330615d74反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-6a295f1bf62b427b8bb361fd84047ff1反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-c4ac6ef2103540e794ccd64403e63146反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-d71ad6bcde594558b593c1b1712656bf反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Preparation of 2-(3-methyl-n-butyl)-indole. Carbonyldiimidazole (65 g) was mixed with 500 ml of dry dichloromethane in a 2-L round bottom flask and stirred magnetically. A solution of 4-methylvaleric acid in 200 ml of dichloromethane was added dropwise over 45 minutes and the mixture was stirred for another 1.25 hours. o-Toluidine (45 g) in 100 ml of dichloromethane was then added over about 20 minutes. After stirring for 2 hours the mixture was washed with water and then the solvent was stripped on a rotary evaporator. The residue was mixed with 150 ml of methanol and 75 ml of water and put in the freezer. Filtration of the precipitate, dilution of the filtrate with water and refiltration of the precipitate gave 75 g (94%) of vacuum dried N-(2-methylphenyl)-4-methylvaleramide which was used without further treatment in the next step. the mixture was stirred for another 1.25 hours After stirring for 2 hours the mixture was washed with water the solvent was stripped on a rotary evaporator The residue was mixed with 150 ml of methanol and 75 ml of water Filtration of the precipitate, dilution of the filtrate with water and refiltration of the precipitate
ソース ID: ord-9ed715a2df7c47048f4b78f4d6d76603反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: The title compound, white solid (77 mg, 73%), MS (ISP) m/z=427.4 [(M+H)+], mp 188° C., was prepared in accordance with the general method of example 1 from trans-4-{2-[4-(2,3-dihydro-benzofuran-4-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine dihydro chloride (intermediate B) (100 mg, 0.25 mmol) and 4-methyl-pentanoic acid.
ソース ID: ord-92788f0c3c3d4a70a739237458b56421反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b08797dbc1b1416db51be7c3593bd6f2反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-473296d1fc664c1c92554b740ad09caePubChem 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。
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