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Diisobutylaluminumhydride → (1-benzyl-2-chloro-5-phenyl-1H-pyrrol-3-yl)methanol

HRID 505822
ノート
印刷プレビュー

反応式

HRID 505822 の反応式
[CH2:1]([N:8]1[C:12]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[CH:11][C:10]([C:19](OC)=[O:20])=[C:9]1[Cl:23])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].C([Al+]CC(C)C)C(C)C>C(Cl)Cl>[CH2:1]([N:8]1[C:12]([C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)=[CH:11][C:10]([CH2:19][OH:20])=[C:9]1[Cl:23])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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 21225700DiisobutylaluminumhydrideHCID 68468834methyl 1-benzyl-2-chloro-5-phenyl-1H-pyrrole-3-carboxylate

生成物 1

HCID 68472482(1-benzyl-2-chloro-5-phenyl-1H-pyrrol-3-yl)methanol収率 90%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-78 °C

実験手順

A solution (0.24 M) of methyl 1-benzyl-2-chloro-5-phenyl-1H-pyrrole-3-carboxylate in DCM at −78° C. was treated with diisobutylaluminium hydride (1 M solution in DCM, 2.5 eq.). The resulting solution was stirred at −78° C. for 2 h then it was warmed to 0° C. and quenched with MeOH. The Rochelle solution (10% wt sodium and potassium tartrate) was added and the mixture was stirred at RT for 1 h (until two phases came out). The mixture was extracted with DCM and the combined organic phase was treated with brine and dried. Evaporation of the solvent afforded the title compound (90%) as an oil.

後処理

  1. temperatureit was warmed to 0° C.
  2. customquenched with MeOH
  3. additionThe Rochelle solution (10% wt sodium and potassium tartrate) was added
  4. stirringthe mixture was stirred at RT for 1 h (until two phases came out)
  5. extractionThe mixture was extracted with DCM
  6. additionthe combined organic phase was treated with brine
  7. customdried
  8. customEvaporation of the solvent

出典と根拠

ORDレコード
ord-16dd888a92e04b4d9379ffdca2aa657b
出典データセット
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07781431B2

反応ノート

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