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

HRID 505822
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HRID 505822 반응식
[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
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참가 물질

4

반응물 2

HCID 21225700DiisobutylaluminumhydrideHCID 68468834methyl 1-benzyl-2-chloro-5-phenyl-1H-pyrrole-3-carboxylate

생성물 1

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

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
-78 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-16dd888a92e04b4d9379ffdca2aa657b
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07781431B2

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