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2-Chlorocyclopentanone → 2-acetoxymethyl-5,6-dihydro-4H-cyclopentathiazole

HRID 1654177
ノート
印刷プレビュー

反応式

HRID 1654177 の反応式
[C:1]([O:4][CH2:5][C:6]([NH2:8])=[S:7])(=[O:3])[CH3:2].Cl[CH:10]1[CH2:14][CH2:13][CH2:12][C:11]1=O>CN(C)C=O>[C:1]([O:4][CH2:5][C:6]1[S:7][C:10]2[CH2:14][CH2:13][CH2:12][C:11]=2[N:8]=1)(=[O:3])[CH3:2]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 127512-ChlorocyclopentanoneHCID 11018908Carbamothioylmethyl acetate

生成物 1

HCID 677578922-acetoxymethyl-5,6-dihydro-4H-cyclopentathiazole収率 33.8%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
80 °C

実験手順

A mixture of 2-acetoxythioacetamide (10 g), 2-chlorocyclopentanone (10.6 g) and dimethylformamide (100 ml) was stirred for 24 hours at 80° C. The reaction mixture was cooled and poured into ice-water (500 ml), followed by extraction twice with ethyl acetate (200 ml). The extract was washed twice with water (100 ml), which was dried over magnesium sulfate, then the solvent was distilled off under reduced pressure. The residue was subjected to a silica gel chromatography (2.5×50 cm), eluting with ethyl acetate-hexane (3:7). The object fraction was concentrated to give 2-acetoxymethyl-5,6-dihydro-4H-cyclopentathiazole (5 g) as a yellow oily product.

後処理

  1. temperatureThe reaction mixture was cooled
  2. extractionfollowed by extraction twice with ethyl acetate (200 ml)
  3. washThe extract was washed twice with water (100 ml), which
  4. dry with materialwas dried over magnesium sulfate
  5. distillationthe solvent was distilled off under reduced pressure
  6. washeluting with ethyl acetate-hexane (3:7)
  7. concentrationThe object fraction was concentrated

出典と根拠

ORDレコード
ord-688df7a317ff428e8eb86212c13c335c
出典データセット
uspto-grants-1995_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05405861

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート