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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 2-Amino-3-(3,4,5-trifluorophenyl)propanoic acid hydrochloride

HRID 1359909
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HRID 1359909 반응식
C([O:3][C:4](=[O:30])[CH:5]([CH2:20][C:21]1[CH:26]=[C:25]([F:27])[C:24]([F:28])=[C:23]([F:29])[CH:22]=1)[N:6]=C(C1C=CC=CC=1)C1C=CC=CC=1)C.[ClH:31]>O>[ClH:31].[F:27][C:25]1[CH:26]=[C:21]([CH:22]=[C:23]([F:29])[C:24]=1[F:28])[CH2:20][CH:5]([C:4]([OH:30])=[O:3])[NH2:6]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 58584141N-(Diphenylmethylene) (3,4,5-trifluoro)-D,L-Phenylalanine ethyl ester

생성물 1

HCID 669639102-Amino-3-(3,4,5-trifluorophenyl)propanoic acid hydrochloride

시약·촉매·용매 1

HCID 962Water용매

실험 절차

N-(Diphenylmethylene) (3,4,5-trifluoro)-D,L-Phenylalanine ethyl ester (1.33 g, 3.2 mmol) was suspended in water (15 mL) at 25° C. and treated with conc. hydrochloric acid (5 mL). The mixture was heated at reflux for 4 hrs and evaporated to dryness. The residue was triturated with diethyl ether (4×20 mL). The solid was filtered and dried to afford title compound (0.72 g)

후처리

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 4 hrs
  3. customevaporated to dryness
  4. customThe residue was triturated with diethyl ether (4×20 mL)
  5. filtrationThe solid was filtered
  6. customdried

출처 및 근거

ORD 기록
ord-1df43f83820342d6a416547717f5b1e0
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07879795B2

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