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Sodium borohydride → HCID 54562928, 화합물

HRID 1413743
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HRID 1413743 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-63c69a497b394de5b7b1bbeaceb0009b
출처 데이터셋
uspto-grants-1981_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04251454

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