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Hydrochloric Acid → 3-Benzyloxymethyl-3-benzylthiomethylhexan-2-ol

HRID 704151
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HRID 704151 반응식
[CH3:1][Mg]I.[CH2:4]([O:11][CH2:12][C:13]([CH2:19][S:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)([CH2:16][CH2:17][CH3:18])[CH:14]=[O:15])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.Cl>C(OCC)C>[CH2:4]([O:11][CH2:12][C:13]([CH2:19][S:20][CH2:21][C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1)([CH2:16][CH2:17][CH3:18])[CH:14]([OH:15])[CH3:1])[C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 200755792-Benzyloxymethyl-2-benzylthiomethyl-pentanalHCID 178418373HCID 178418373, 화합물

생성물 1

HCID 200755623-Benzyloxymethyl-3-benzylthiomethylhexan-2-ol

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

Methyl magnesium iodide (4.0 ml, 3M solution in ether) was added to a solution of 2-benzyloxymethyl-2-benzylthiomethyl-pentanal (2.6 g.) in dry diethyl ether (50 ml.) at 0°. The mixture was refluxed, with stirring for 2 hours. The mixture was cooled and poured into 1N hydrochloric acid in ice. The aqueous mixture was extracted with diethyl ether. The ethereal extracts were washed with water, dried over anhydrous magnesium sulphate and evaporated in vacuo. The residue was chromatographed on silica, eluting with diethyl ether. 3-Benzyloxymethyl-3-benzylthiomethylhexan-2-ol was obtained as a colourless oil (0.7 g.).

후처리

  1. temperatureThe mixture was refluxed
  2. temperatureThe mixture was cooled
  3. extractionThe aqueous mixture was extracted with diethyl ether
  4. washThe ethereal extracts were washed with water
  5. dry with materialdried over anhydrous magnesium sulphate
  6. customevaporated in vacuo
  7. customThe residue was chromatographed on silica
  8. washeluting with diethyl ether

출처 및 근거

ORD 기록
ord-8c2eed9cae6e45af8702d99b7750eb32
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04985582

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