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1,2,3,4-tetrahydro-6-benzyloxynaphthalene-2-carboxylic acid (R)-1-trifluoromethylheptyl ester → HCID 18655712, 화합물

HRID 1418
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HRID 1418 반응식
[H][H].[F:3][C:4]([F:34])([F:33])[C@H:5]([O:12][C:13]([CH:15]1[CH2:24][CH2:23][C:22]2[C:17](=[CH:18][CH:19]=[C:20]([O:25]CC3C=CC=CC=3)[CH:21]=2)[CH2:16]1)=[O:14])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11]>[Pd].O1CCCC1>[F:3][C:4]([F:33])([F:34])[C@H:5]([O:12][C:13]([CH:15]1[CH2:24][CH2:23][C:22]2[C:17](=[CH:18][CH:19]=[C:20]([OH:25])[CH:21]=2)[CH2:16]1)=[O:14])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 186557111,2,3,4-tetrahydro-6-benzyloxynaphthalene-2-carboxylic acid (R)-1-trifluoromethylheptyl esterHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 18655712HCID 18655712, 화합물수율 100%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8028Tetrahydrofuran용매

실험 절차

Hydrogen gas was blown into a mixture of 8.19 g (18.3 mmol) of the 1,2,3,4-tetrahydro-6-benzyloxynaphthalene-2-carboxylic acid (R)-1-trifluoromethylheptyl ester obtained in the fourth stage, 3.6 g of 5% palladium/carbon as a catalyst and 50 ml of tetrahydrofuran with stirring at room temperature and ordinary pressure for 24 hours. The reaction mixture was filtered using Celite as a filter aid, and the filtrate obtained was concentrated to obtain 6.78 g (18.3 mmol) of 1,2,3,4-tetrahydro-6-hydroxynaphthalene-2-carboxylic acid (R)-1-trifluoromethylheptyl ester as a brown liquid.

후처리

  1. filtrationThe reaction mixture was filtered
  2. customthe filtrate obtained
  3. concentrationwas concentrated

출처 및 근거

ORD 기록
ord-1973f4fcc3e34d7aab97de56c9a9b263
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05725798

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