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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 11528683, 화합물 → (6S)-6-Methyl-7-(tetrahydro-2H-pyran-2-yloxy)heptan-2-one

HRID 2053402
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인쇄 미리보기

반응식

HRID 2053402 반응식
[CH3:1][C@H:2]([CH2:9][O:10][CH:11]1[CH2:16][CH2:15][CH2:14][CH2:13][O:12]1)[CH2:3][C:4]#[C:5][C:6](=[O:8])[CH3:7].[H][H]>[Pd].C1COCC1>[CH3:1][C@H:2]([CH2:9][O:10][CH:11]1[CH2:16][CH2:15][CH2:14][CH2:13][O:12]1)[CH2:3][CH2:4][CH2:5][C:6](=[O:8])[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 11528683HCID 11528683, 화합물HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 11622725(6S)-6-Methyl-7-(tetrahydro-2H-pyran-2-yloxy)heptan-2-one수율 100%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8028Tetrahydrofuran용매

실험 절차

A 50 g solution (222.9 mmol) of (S)-6-methyl-7-[(RS)-(3,4,5,6-tetrahydro-2H-pyran-2-yl)oxy]hept-3-in-2-one and 5 g palladium on carbon (10% Pd/C) in 400 ml of THF is hydrogenated for one hour at 8 bar hydrogen at room temperature. The catalyst is then filtered off, rewashed with little solvent and the solvent is removed in vacuo. 50.9 g of product is obtained.

후처리

  1. filtrationThe catalyst is then filtered off
  2. customthe solvent is removed in vacuo

출처 및 근거

ORD 기록
ord-f341d14b8c8540eabe506c23d45a5a08
출처 데이터셋
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07326798B2

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