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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → Hydrochloric Acid

HRID 1982323
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HRID 1982323 반응식
[NH:1](C(OCC1C=CC=CC=1)=O)[C@H:2]([C@H:7]([CH2:9][C:10]([O:12][CH3:13])=[O:11])[OH:8])[CH2:3][CH:4]([CH3:6])[CH3:5].[ClH:24]>CO.[Pd]>[NH2:1][C@H:2]([C@H:7]([CH2:9][C:10]([O:12][CH3:13])=[O:11])[OH:8])[CH2:3][CH:4]([CH3:6])[CH3:5].[ClH:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 313Hydrochloric AcidHCID 14681745Z-Sta-OMe

생성물 2

HCID 313Hydrochloric AcidHCID 13384495H-Sta-OMe

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

818 mg of Z-Sta-OMe dissolved in 40 ml of methanol are hydrogenated at room temperature and normal pressure in the presence of 190 mg of palladium-on-carbon catalyst (10% Pd) until saturation. During hydrogenation, the pH value is maintained constantly at 5 by the continuous addition of 0.5N HCl. After hydrogenation the catalyst is filtered off and the filtrate is concentrated by evaporation. H-Sta-OMe×HCl is obtained in the form of a colourless foam; Rf (G)=0.21. This crude product is used directly in stage 13.5.

후처리

  1. customare hydrogenated at room temperature
  2. filtrationAfter hydrogenation the catalyst is filtered off
  3. concentrationthe filtrate is concentrated by evaporation

출처 및 근거

ORD 기록
ord-f87b1843194a4ef3b0919d06a97d2a60
출처 데이터셋
uspto-grants-1986_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04595677

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