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Methanol → HCID 13362007, 화합물

HRID 1632606
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HRID 1632606 반응식
[CH2:1]([N:8]1[C:12](=[O:13])[CH2:11][CH:10]([C:14](OC)=[O:15])[CH:9]1[C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([O:24][CH3:25])[CH:19]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CO.[BH4-].[Na+]>O>[CH2:1]([N:8]1[CH:9]([C:18]2[CH:23]=[CH:22][CH:21]=[C:20]([O:24][CH3:25])[CH:19]=2)[CH:10]([CH2:14][OH:15])[CH2:11][C:12]1=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 4311764Sodium borohydrideHCID 13362006HCID 13362006, 화합물

생성물 1

HCID 13362007HCID 13362007, 화합물

시약·촉매·용매 1

HCID 962Water용매

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온도
50 °C

실험 절차

To 42.1 gm. of methyl 1-benzyl-2-(3-methoxyphenyl)-5-oxopyrrolidin-3-carboxylate in 436 ml. of absolute methanol was slowly added at -10° to -5°, 37.9 gm. of sodium borohydride. The reaction mixture was left in the ice bath until it came to ambient temperature. Concentration in vacuo provided a white gum which was suspended in water and heated to 50° C. The gum was extracted with chloroform, dried (Na2SO4), filtered, and concentrated in vacuo to yield 22.8 gm. of yellow oil.

후처리

  1. customcame to ambient temperature
  2. concentrationConcentration in vacuo
  3. customprovided a white gum which
  4. extractionThe gum was extracted with chloroform
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customto yield 22.8 gm

출처 및 근거

ORD 기록
ord-8a0891f21c83439595e67f2e903b95d3
출처 데이터셋
uspto-grants-1984_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04476311

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