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Acetic Acid → HCID 13293071, 화합물

HRID 904820
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HRID 904820 반응식
[C:1]([NH:4][CH:5]1[CH2:14][CH2:13][C:12]2[C:7](=[CH:8][C:9]([O:15][CH3:16])=[CH:10][CH:11]=2)[C:6]1=[O:17])(=[O:3])[CH3:2].[BH4-].[Na+].C(O)(=O)C.CCOCC>C(O)C>[C:1]([NH:4][C@@H:5]1[CH2:14][CH2:13][C:12]2[C:7](=[CH:8][C:9]([O:15][CH3:16])=[CH:10][CH:11]=2)[C@H:6]1[OH:17])(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 3283Diethyl EtherHCID 4311764Sodium borohydride2회HCID 13435388HCID 13435388, 화합물

생성물 1

HCID 13293071HCID 13293071, 화합물수율 35%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a stirred solution of 2-acetamido-7-methoxy-3,4-dihydronaphthalen 1(2H)-one in absolute ethanol (100 ml) was added sodium borohydride (1.6 gms, 0.04 m) in portions. After stirring for 1/2 hour, acetic acid was added to decompose any excess sodium borohydride. The reaction mixture was poured onto water (150 ml) and this was extracted with ethyl acetate (3×150). The ethyl acetate was washed with aqueous saturated sodium chloride, and was dried over anhydrous sodium sulfate. After filtration, the ethyl acetate was removed under reduced pressure (20 mm) to give a semisolid. The solid was slurried with ether and filtered to yield 3.3 gms (35%) of product as a white solid, m.p. 135°-140° C.

후처리

  1. additionThe reaction mixture was poured onto water (150 ml)
  2. extractionthis was extracted with ethyl acetate (3×150)
  3. washThe ethyl acetate was washed with aqueous saturated sodium chloride
  4. dry with materialwas dried over anhydrous sodium sulfate
  5. filtrationAfter filtration
  6. customthe ethyl acetate was removed under reduced pressure (20 mm)
  7. customto give a semisolid
  8. filtrationfiltered

출처 및 근거

ORD 기록
ord-505e05079b074c3fb210d1b77d465fab
출처 데이터셋
uspto-grants-1983_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04420480

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