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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → (S)-2-Amino-3-cyclohexylpropanoic acid hydrochloride

HRID 2380116
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HRID 2380116 반응식
[NH2:1][C@H:2]([C:10]([OH:12])=[O:11])[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[H][H].O.[ClH:16]>[Pt]>[CH2:7]1[CH2:6][CH2:5][CH:4]([CH2:3][C@H:2]([NH2:1])[C:10]([OH:12])=[O:11])[CH2:9][CH2:8]1.[ClH:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 6140L-PhenylalanineHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 23381533(S)-2-Amino-3-cyclohexylpropanoic acid hydrochloride수율 91%

시약·촉매·용매 1

HCID 23939Platinum촉매

실험 절차

A solution of 10.4 g (61.7 mmoles) of L-phenylalanine in 150 ml of 2N aqueous hydrochloric acid was subjected to a medium pressure catalytic hydrogenation reaction in the presence of 1 g of platinum black using a Paar's apparatus under about 4 atmospheres of hydrogen at room temperature for 24 hours. At the end of this time, the precipitated crystalline substance was dissolved by adding 250 ml of water, and the catalyst was removed by filtration. The filtrate was then concentrated to about 150 ml by evaporation under reduced pressure and allowed to stand overnight. The crystalline substance which deposited was collected by filtration and dried to give 12.8 g (yield 91%) of the title compound as white crystals, melting at 232°-234° C.

후처리

  1. dissolutionAt the end of this time, the precipitated crystalline substance was dissolved
  2. customthe catalyst was removed by filtration
  3. concentrationThe filtrate was then concentrated to about 150 ml by evaporation under reduced pressure
  4. filtrationThe crystalline substance which deposited was collected by filtration
  5. customdried

출처 및 근거

ORD 기록
ord-3b421810ad4a400b9d633cafd45b7f04
출처 데이터셋
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05364844

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