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Methanesulfonyl chloride → HCID 13603621, 화합물

HRID 1722836
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반응식

HRID 1722836 반응식
[CH3:1][O:2][C:3]1[CH:15]=[CH:14][CH:13]=[CH:12][C:4]=1[O:5][CH2:6][CH:7]1[NH:11][CH2:10][CH2:9][S:8]1.[CH3:16][S:17](Cl)(=[O:19])=[O:18]>N1C=CC=CC=1.OS(O)(=O)=O>[CH3:16][S:17]([N:11]1[CH2:10][CH2:9][S:8][CH:7]1[CH2:6][O:5][C:4]1[CH:12]=[CH:13][CH:14]=[CH:15][C:3]=1[O:2][CH3:1])(=[O:19])=[O:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 31297Methanesulfonyl chlorideHCID 30254542-[(2-Methoxyphenoxy)methyl]-1,3-thiazolidine

생성물 1

HCID 13603621HCID 13603621, 화합물수율 89.3%

시약·촉매·용매 2

HCID 1049Pyridine용매HCID 1118Sulfuric Acid용매

실험 절차

A solution of 2-(o-methoxyphenoxy)methyl-thiazolidine (1.83 g) in pyridine (6 ml) is treated with methane sulphonyl chloride (1.2 g) at room temperature. After 4 hours the mixture is diluted with 2N H2SO4, extracted with Et2O, to afford after the usual work-up 2.2 g of 3-methanesulphonyl-2-(o-methoxyphenoxy)methyl-thiazolidine m.p. 118°-120° C.

후처리

  1. extractionextracted with Et2O

출처 및 근거

ORD 기록
ord-b604238656cf439e8cade8f13ebf50be
출처 데이터셋
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04857643

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