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4-Oxononanoic acid → HCID 54023284, 화합물

HRID 2304949
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HRID 2304949 반응식
[O:1]=[C:2]([CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])[CH2:3][CH2:4][C:5]([OH:7])=[O:6].[CH3:13][C:14](=[CH:16][CH2:17][CH2:18]/[C:19](=[CH:21]/[CH2:22]O)/[CH3:20])[CH3:15]>ClCCl.N1(C2C=CN=CC=2)CCCC1>[CH3:20][C:19]([CH2:18][CH2:17][CH:16]=[C:14]([CH3:15])[CH3:13])=[CH:21][CH2:22][O:6][C:5](=[O:7])[CH2:4][CH2:3][C:2](=[O:1])[CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 224334-Oxononanoic acidHCID 637566Geraniol

생성물 1

HCID 54023284HCID 54023284, 화합물수율 59.7%

시약·촉매·용매 2

HCID 755674-Pyrrolidinopyridine촉매HCID 6344Dichloromethane용매

실험 절차

A solution of 20 g 4-oxo-nonanoic acid, 19.3 g geraniol, 26.8 g N,N-dicyclohexyl-carbodiimide and 1.0 g 4-pyrrolidinopyridine in 300 ml of dichloromethane was stirred for 24 hours at room temperature. The precipitate was filtered off, the filtrate was diluted with ether, washed with aqueous hydrochloric acid, saturated NaHCO3 and brine. The organic phase was dried, filtered and evaporated to dryness. The resulting oil-crystal mixture was purified by chromatography to yield 21.4 g of a colorless oil.

후처리

  1. filtrationThe precipitate was filtered off
  2. additionthe filtrate was diluted with ether
  3. washwashed with aqueous hydrochloric acid, saturated NaHCO3 and brine
  4. customThe organic phase was dried
  5. filtrationfiltered
  6. customevaporated to dryness
  7. customThe resulting oil-crystal mixture was purified by chromatography

출처 및 근거

ORD 기록
ord-4197acffa2c442a8b35eacf182f34cd1
출처 데이터셋
uspto-grants-2002_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06437150B1

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