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Methanol → 7-Bromoheptanal

HRID 67655
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HRID 67655 반응식
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]
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참가 물질

7

반응물 4

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

생성물 1

HCID 124703357-Bromoheptanal수율 85.3%

시약·촉매·용매 2

HCID 1140Toluene용매
HCID 6344
Dichloromethane
용매

실험 절차

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:

후처리

  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

출처 및 근거

ORD 기록
ord-26d3bd2635924f5d8c9669e11ae3ebee
출처 데이터셋
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04346099

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