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Acetic Acid → HCID 22620115, 화합물

HRID 840617
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HRID 840617 반응식
C(O[C:4](=[O:20])[CH2:5][CH:6]1[CH2:11][CH:10]([CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:9][CH2:8][C:7]1=O)C.C(O)(=O)C.[CH2:25]([NH2:32])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C(Cl)(Cl)Cl.C([O-])([O-])=O.[Na+].[Na+].ClCCCl>[CH2:25]([N:32]1[CH:7]2[CH:6]([CH2:11][CH:10]([CH2:12][C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=3)[CH2:9][CH2:8]2)[CH2:5][C:4]1=[O:20])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 176Acetic AcidHCID 7504BenzylamineHCID 5049666Sodium triacetoxyborohydrideHCID 69940430HCID 69940430, 화합물

생성물 1

HCID 22620115HCID 22620115, 화합물수율 53.7%

시약·촉매·용매 3

HCID 111,2-Dichloroethane용매
HCID 6212
Chloroform
용매
HCID 10340Sodium Carbonate용매

실험 절차

A mixture of 8 g of (5-benzyl-2-oxo-cyclohexyl)-acetic acid ethyl ester, 3.4 g of acetic acid, 3.75 g of benzylamine, 50 mL of 1,2-dichloroethane and 7.7 g of sodium triacetoxyborohydride was stirred at room temperature for 48 h. The reaction mixture was diluted with 100 mL chloroform and 40 mL saturated aqueous Na2CO3 and the layers separated. The aqueous layer was extracted with 2×25 mL of chloroform and the combined organic layers dried over magnesium sulfate and concentrated under reduced pressure. Purification by chromatography eluting with 50% ethyl acetate in hexane gave 5 g of 1,5-dibenzyl-octahydro-indol-2-one.

후처리

  1. customthe layers separated
  2. extractionThe aqueous layer was extracted with 2×25 mL of chloroform
  3. dry with materialthe combined organic layers dried over magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customPurification by chromatography
  6. washeluting with 50% ethyl acetate in hexane

출처 및 근거

ORD 기록
ord-7ce01fd0f88b48f2b1c404653fc994df
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06369076B1

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