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Trichloroacetic Acid → 5-Methoxy-2,6-dimethylheptan-1-ol

HRID 435780
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인쇄 미리보기

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HRID 435780 반응식
C[O:2][CH:3](OC)[CH:4]([CH3:13])[CH2:5][CH2:6][CH:7]([O:11][CH3:12])[CH:8]([CH3:10])[CH3:9].ClC(Cl)(Cl)C(O)=O.[OH-].[Na+].[BH4-].[Na+]>CO.O.O1CCCC1>[OH:2][CH2:3][CH:4]([CH3:13])[CH2:5][CH2:6][CH:7]([O:11][CH3:12])[CH:8]([CH3:9])[CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 6421Trichloroacetic AcidHCID 14798Sodium HydroxideHCID 4311764Sodium borohydrideHCID 213990641,1,5-Trimethoxy-2,6-dimethylheptane

생성물 1

HCID 213991185-Methoxy-2,6-dimethylheptan-1-ol

시약·촉매·용매 3

HCID 887Methanol용매
HCID 962
Water
용매
HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 10.9 g. of 1,1,5-trimethoxy-2,6-dimethylheptane in 200 ml. of tetrahydrofuran and 60 ml. of water is treated with one g. of trichloroacetic acid and then the mixture heated at 60° for one hour. After cooling, there is added 40 ml. of 2N sodium hydroxide in methanol followed by 2 g. of powdered sodium borohydride. The reaction mixture is stirred at room temperature for three hours and then concentrated and extracted with ether. The ethereal extracts are evaporated under reduced pressure to give crude 1-hydroxy-5-methoxy-2,6-dimethylheptane which can be purified by distillation.

후처리

  1. temperatureAfter cooling
  2. additionthere is added 40 ml
  3. concentrationconcentrated
  4. extractionextracted with ether
  5. customThe ethereal extracts are evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-5db090211beb439c9181f8b2b1da84d8
출처 데이터셋
uspto-grants-1977_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04006188

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