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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Acid → HCID 11841701, 화합물

HRID 904822
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HRID 904822 반응식
[C:1]([NH:4][CH:5]1[CH2:14][CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]1=[O:15])(=[O:3])[CH3:2].[BH4-].[Na+].C(O)(=O)C>C(O)C>[C:1]([NH:4][C@@H:5]1[CH2:14][CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C@H:6]1[OH:15])(=[O:3])[CH3:2]
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참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 4311764Sodium borohydrideHCID 9859076HCID 9859076, 화합물

생성물 1

HCID 11841701HCID 11841701, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of the 2-acetamido-3,4-dihydronaphthalen-1(2H)-one from Step A in absolute ethanol (150 ml) was added sodium borohydride (2.0 gms, 0.05 m) in portions. The reaction mixture was stirred at room temperature for 1/2 hour. Acetic acid was added dropwise to destroy the excess sodium borohydride. The reaction mixture was poured into water and extracted with ethyl acetate (3×150 ml). The ethyl acetate was washed with saturated aqueous sodium chloride (150 ml) and dried over anhydrous sodium sulfate. After filtration the solvent was removed under reduced pressure to yield 5.5 gms (54%, over Steps A and B), of product as a solid.

후처리

  1. customto destroy the excess sodium borohydride
  2. additionThe reaction mixture was poured into water
  3. extractionextracted with ethyl acetate (3×150 ml)
  4. washThe ethyl acetate was washed with saturated aqueous sodium chloride (150 ml)
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationAfter filtration the solvent
  7. customwas removed under reduced pressure
  8. customto yield 5.5 gms (54%, over Steps A and B)

출처 및 근거

ORD 기록
ord-be04bfdb20004457acb2cd6e96904541
출처 데이터셋
uspto-grants-1983_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04420480

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