tert-Butoxy bis(dimethylamino)methane → HCID 67406834、化合物

HRID 643747ノート

反応式

HRID 643747 の反応式
[C:1]([Si:5]([CH3:15])([CH3:14])[O:6][C:7]1[C:8](=[O:13])[CH2:9][CH2:10][CH2:11][CH:12]=1)([CH3:4])([CH3:3])[CH3:2].CC(O[CH:21](N(C)C)[N:22]([CH3:24])[CH3:23])(C)C>C1(C)C=CC=CC=1>[C:1]([Si:5]([CH3:15])([CH3:14])[O:6][C:7]1[C:8](=[O:13])[C:9](=[CH:21][N:22]([CH3:24])[CH3:23])[CH2:10][CH2:11][CH:12]=1)([CH3:4])([CH3:3])[CH3:2]

参加物

4

反応物 2

HCID 79885tert-Butoxy bis(dimethylamino)methaneHCID 117463392-Cyclohexen-1-one, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-

生成物 1

HCID 67406834HCID 67406834、化合物

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

反応条件

温度
115 °C

実験手順

A mixture of 2-(tert-butyl-dimethyl-silanyloxy)-cyclohex-2-enone (6.9 g, 30.48 mmol) in dry toluene (50 mL) was treated with Bredereck's reagent (9.44 ml, 45.72 mmol) was stirred at 115° C. for 24 hours. The mixture was concentrated under reduced pressure to give 2-(tert-butyl-dimethyl-silanyloxy)-6-dimethylaminomethylene-cyclohex-2-enone as a semi-solid brown residue which was used as such in the next step.

後処理

  1. concentrationThe mixture was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-c63bf9ca5e094c6dad020506e4959847
出典データセット
uspto-grants-2010_04
特許番号
US07700609B2

反応ノート

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