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Ethanol → 2-Methyl-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carbonitrile

HRID 2371048
ノート
印刷プレビュー

反応式

HRID 2371048 の反応式
[CH3:1][C:2]1[S:3][C:4]2[C:10](=O)[CH2:9][CH2:8][CH2:7][C:5]=2[N:6]=1.CC1C=CC(S([CH2:22][N+:23]#[C-])(=O)=O)=CC=1.C(O)C.CC([O-])(C)C.[K+]>COCCOC>[CH3:1][C:2]1[S:3][C:4]2[CH:10]([C:22]#[N:23])[CH2:9][CH2:8][CH2:7][C:5]=2[N:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 702EthanolHCID 161915Tosylmethyl isocyanideHCID 149133692-Methyl-5,6-dihydrobenzo[d]thiazol-7(4H)-oneHCID 23665647Potassium tert-butoxide

生成物 1

HCID 672573622-Methyl-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carbonitrile

試薬・触媒・溶媒 1

HCID 80711,2-Dimethoxyethane
溶媒

実験手順

To a stirred and cooled solution of 5,6-dihydro-2-methylbenzo[d]thiazol-7(4H)-one (1.67 g, 10 mmol) and TOSMIC (2.5 g, 13 mmol) in a mixture of DME (25 mL) and absolute ethanol (25 mL) was added solid t-BuOK (2.8 g, 24 mmol) portionwise while keeping the reaction temperature between 5 and 10° C. The resulting mixture was stirred at room temperature for 30 minutes and at 30-45° C. for 30 minutes. The resulting suspension was cooled to room temperature. The precipitate (TosK) was removed by filtration and rinsed with DME. The combined DME solutions were concentrated under reduced pressure to give the crude product, which was purified by column chromatography.

後処理

  1. customthe reaction temperature between 5 and 10° C
  2. stirringThe resulting mixture was stirred at room temperature for 30 minutes and at 30-45° C. for 30 minutes
  3. customThe precipitate (TosK) was removed by filtration
  4. washrinsed with DME
  5. concentrationThe combined DME solutions were concentrated under reduced pressure

出典と根拠

ORDレコード
ord-33190a766f104e7a9c9532481b7f2d87
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08710245B2

反応ノート

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