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Methanol → 4-Benzyloxy-3-ethylsulfinylphenol

HRID 23566
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반응식

HRID 23566 반응식
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][C:10]=1[S:16]([CH3:18])=[O:17])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:19]([N-]C(C)C)(C)C.[Li+].CI.CO>O1CCCC1>[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][C:10]=1[S:16]([CH2:18][CH3:19])=[O:17])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 887MethanolHCID 6328Methyl iodideHCID 2724682Lithium diisopropylamideHCID 225744604-Benzyloxy-3-methylsulfinylphenol

생성물 1

HCID 225744554-Benzyloxy-3-ethylsulfinylphenol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 0.4 g of 4-benzyloxy-3-methylsulfinylphenol pmb (1.05 mmol) in 40 ml of tetrahydrofuran is cooled to −50° C. and 0.784 ml of a dimolar solution of lithium diisopropylamide (1.57 mmol) in tetrahydrofuran is then added. The reaction mixture is stirred for 15 minutes and 0.13 ml of methyl iodide (1.1 mmol) is added. After stirring for 15 minutes, methanol is added and the solvents are evaporated off under reduced pressure. The 4-benzyloxy-3-ethylsulfinylphenol pmb is obtained in the form of a white solid (0.3 g, 72%) after purification on silica gel (40 g SiO2, eluent: 4/1 heptane/ethyl acetate)

후처리

  1. stirringAfter stirring for 15 minutes
  2. customthe solvents are evaporated off under reduced pressure

출처 및 근거

ORD 기록
ord-ddd2918f70da4a6ca26f83d6f354b3bb
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06852736B2

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