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Sodium borohydride → HCID 54562928, 화합물

HRID 441312
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HRID 441312 반응식
[BH4-].[Na+].[CH3:3][NH:4][C:5]1[CH:6]=[C:7]([C:13](=[O:19])[CH2:14][S:15]([CH3:18])(=[O:17])=[O:16])[CH:8]=[C:9]([NH:11][CH3:12])[CH:10]=1>C(O)C>[CH3:3][NH:4][C:5]1[CH:6]=[C:7]([CH:8]=[C:9]([NH:11][CH3:12])[CH:10]=1)[CH:13]([OH:19])[CH2:14][S:15]([CH3:18])(=[O:17])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 202903761-[3,5-Bis(methylamino)phenyl]-2-(methanesulfonyl)ethan-1-one

생성물 1

HCID 54562928HCID 54562928, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A suspension of 7.6 g. of sodium borohydride and 12.8 g. of 3',5'-bis-(methylamino)-2-methylsulfonylacetophenone in 200 ml. of ethanol was stirred for 18 hours at 25° C. After the addition of 50 ml. of water, the solution was evaporated to dryness in vacuo. The residue was heated to boiling in 300 ml. of ethyl acetate. The insoluble material was separated and the filtrate evaporated to dryness in vacuo. Recrystallization of the residue from ethanol gave 3,5-bis-(methylamino)- α -[(methylsulfonyl)methyl]benzyl alcohol, having a melting point of 106° C.

후처리

  1. additionA suspension of 7.6 g
  2. additionAfter the addition of 50 ml
  3. customof water, the solution was evaporated to dryness in vacuo
  4. temperatureThe residue was heated
  5. customThe insoluble material was separated
  6. customthe filtrate evaporated to dryness in vacuo
  7. customRecrystallization of the residue from ethanol

출처 및 근거

ORD 기록
ord-2401d50df0c54e1ba0f3eae97c4da2cf
출처 데이터셋
uspto-grants-1977_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04039543

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