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4'-Mercaptoacetophenone ethylene acetal → 1-(4-Sulfanylphenyl)ethan-1-one

HRID 1729353
ノート
印刷プレビュー

反応式

HRID 1729353 の反応式
C1O[C:4]([C:6]2[CH:11]=[CH:10][C:9]([SH:12])=[CH:8][CH:7]=2)([CH3:5])[O:3]C1>C(O)CO>[SH:12][C:9]1[CH:10]=[CH:11][C:6]([C:4](=[O:3])[CH3:5])=[CH:7][CH:8]=1
参加物実験手順出典と根拠反応ノート

参加物

3

反応物 1

HCID 189960704'-Mercaptoacetophenone ethylene acetal

生成物 1

HCID 47131801-(4-Sulfanylphenyl)ethan-1-one

試薬・触媒・溶媒 1

HCID 174Ethylene Glycol溶媒

実験手順

4'-Mercaptoacetophenone ethylene acetal (0.656 g; obtained by the reaction of 4'-mercaptoacetophenone and ethylene glycol using an analogous procedure to that described in the third paragraph of the portion of Example 7 which is concerned with the preparation of starting materials) was added to a mixture of 2,4-dibromothiazole (0.82 g), potassium carbonate (0.468 g) and NMP (4 ml). The mixture was stirred and heated to 90° C. for 2.5 hours. The mixture was cooled to ambient temperature and partitioned between diethyl ether and brine. The organic phase was dried (MgSO4) and evaporated. The mixture was purified by column chromatography using a 3:1 mixture of ethyl acetate and petroleum ether as eluent. There was thus obtained 4'-[4-bromothiazol-2-ylthio]acetophenone ethylene acetal (1.1 g, 90%), m.p. 71° C.

出典と根拠

ORDレコード
ord-6beb0fa61dc146658ee0e5251f863f73
出典データセット
uspto-grants-1994_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05332757

反応ノート

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