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2,4,5-Trimethoxybenzaldehyde → N-cyclohexyl-N-cyclopentyl-4-[hydroxy(2,4,5-trimethoxyphenyl)methyl]benzamide

HRID 1588929
ノート
印刷プレビュー

反応式

HRID 1588929 の反応式
Br[C:2]1[CH:21]=[CH:20][C:5]([C:6]([N:8]([CH:14]2[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)[CH:9]2[CH2:13][CH2:12][CH2:11][CH2:10]2)=[O:7])=[CH:4][CH:3]=1.C([Li])(C)(C)C.[CH3:27][O:28][C:29]1[CH:36]=[C:35]([O:37][CH3:38])[C:34]([O:39][CH3:40])=[CH:33][C:30]=1[CH:31]=[O:32]>C1COCC1>[CH:14]1([N:8]([CH:9]2[CH2:13][CH2:12][CH2:11][CH2:10]2)[C:6](=[O:7])[C:5]2[CH:20]=[CH:21][C:2]([CH:31]([OH:32])[C:30]3[CH:33]=[C:34]([O:39][CH3:40])[C:35]([O:37][CH3:38])=[CH:36][C:29]=3[O:28][CH3:27])=[CH:3][CH:4]=2)[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 205252,4,5-TrimethoxybenzaldehydeHCID 197548884-bromo-N-cyclohexyl-N-cyclopentylbenzamideHCID 178418306HCID 178418306、化合物

生成物 1

HCID 19754870N-cyclohexyl-N-cyclopentyl-4-[hydroxy(2,4,5-trimethoxyphenyl)methyl]benzamide

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a cold (-70° C.), stirred solution of 4-bromo-N-cyclohexyl-N-cyclopentylbenzamide (1.5 g, 4.3 mmol) in THF (20 ml) was added slowly a solution of tertbutyllithium (5 ml of 1.7 M solution in pentane) under an Argon atmosphere. The reaction was stirred at -70° to -75° for 20 min. and a solution of 2,4,5-trimethoxybenzaldehyde (843 mg, 4.3 mmol) in THF (10 ml) was added dropwise over 30 min. The reaction was stirred at -70° to -75° for 30 min. and at room temperature for 1 hr. The reaction was quenched by the addition of water and the aqueous layer extracted three times with ethyl acetate. The combined organic layers were washed with water and dried (Na2SO4). The drying agent was filtered and the filtrate concentrated in vacuo to give the crude product. Purification was effected by chromatography on silica gel using mixtures of ethyl acetate and hexane. The product was isolated as a glass.

後処理

  1. stirringThe reaction was stirred at -70° to -75° for 30 min. and at room temperature for 1 hr
  2. customThe reaction was quenched by the addition of water
  3. extractionthe aqueous layer extracted three times with ethyl acetate
  4. washThe combined organic layers were washed with water
  5. dry with materialdried (Na2SO4)
  6. filtrationThe drying agent was filtered
  7. concentrationthe filtrate concentrated in vacuo

出典と根拠

ORDレコード
ord-5d0d7e9bff4f43be89c0f6c5c292cc33
出典データセット
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05223539

反応ノート

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