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Methanesulfonyl chloride → 4-[4-(Benzyloxy)phenyl]butyl methanesulfonate

HRID 2084368
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반응식

HRID 2084368 반응식
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][CH2:17][CH2:18][OH:19])=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:20][S:21](Cl)(=[O:23])=[O:22]>C(OCC)(=O)C.C(N(CC)CC)C>[CH3:20][S:21]([O:19][CH2:18][CH2:17][CH2:16][CH2:15][C:12]1[CH:11]=[CH:10][C:9]([O:8][CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)=[CH:14][CH:13]=1)(=[O:23])=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 31297Methanesulfonyl chlorideHCID 153287654-(Phenylmethoxy)benzenebutanol

생성물 1

HCID 227333684-[4-(Benzyloxy)phenyl]butyl methanesulfonate

시약·촉매·용매 2

HCID 8471Triethylamine용매HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 4-(4-benzyloxyphenyl)butanol (10 g) in ethyl acetate (390 ml), triethylamine (8.16 ml) and methanesulfonyl chloride (4.53 ml) were added drop by drop under ice cooling. After stirring at the ice cooling temperature for 30 minutes and at room temperature for 1 hour, the reaction mixture was washed with ice water and saturated saline. After drying with anhydrous sodium sulfate, the solvent was distilled off under reduced pressure to yield the titled compound (14 g) as an oily substance. This product was used for the next process without purification.

후처리

  1. washthe reaction mixture was washed with ice water and saturated saline
  2. dry with materialAfter drying with anhydrous sodium sulfate
  3. distillationthe solvent was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-1e678630ecc8480e92a1fb9d317dbcd1
출처 데이터셋
uspto-grants-2004_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06716863B2

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