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Methanol → 7-Bromoheptanal

HRID 67655
ノート
印刷プレビュー

反応式

HRID 67655 の反応式
C([O:5][C:6](=O)[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][Br:13])(C)(C)C.[H-].CO.O>C(Cl)Cl.C1(C)C=CC=CC=1>[Br:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH:6]=[O:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 887MethanolHCID 962WaterHCID 166653HydrideHCID 13756138tert-Butyl 7-bromoheptanoate

生成物 1

HCID 124703357-Bromoheptanal収率 85.3%

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒HCID 6344
Dichloromethane
溶媒

実験手順

To 8.5 g of 7-bromoheptanoic acid t-butyl ester (prepared as described in Reference Example 1) in 80 ml of methylene chloride was added dropwise 18.2 ml of a 25% solution of diisobutyl alminium hydride in toluene at -78° C. over a period of 1 hours. The solution was stirred at the same temperature, to which was added 5 ml of methanol at from 0° C. to 10° C. and then added 10 ml of water, and the mixture was stirred at 30° C. to 40° C. for 1 hour. The deposited crystals were filtered out, and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixture of methylene and chloride and cyclohexane (1:1) as an eluent to give 5.28 g of the title compound having the following physical characteristic:

後処理

  1. stirringthe mixture was stirred at 30° C. to 40° C. for 1 hour
  2. filtrationThe deposited crystals were filtered out
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. customThe residue was purified by column chromatography on silica gel using
  5. additiona mixture of methylene and chloride and cyclohexane (1:1) as an eluent

出典と根拠

ORDレコード
ord-26d3bd2635924f5d8c9669e11ae3ebee
出典データセット
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04346099

反応ノート

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