HCID 21667321, 화합물 → HCID 67918842, 화합물

HRID 728874노트

반응식

HRID 728874 반응식
C[O:2][C:3](=[O:25])[CH:4]([NH:22]C=O)/[CH:5]=[C:6](\[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)/[CH2:7][P:8]([O:13]CC)([O:10]CC)=[O:9]>Cl>[NH2:22][CH:4](/[CH:5]=[C:6](\[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)/[CH2:7][P:8]([OH:13])([OH:10])=[O:9])[C:3]([OH:25])=[O:2]

참가 물질

3

반응물 1

HCID 21667321HCID 21667321, 화합물

생성물 1

HCID 67918842HCID 67918842, 화합물

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

0.15 g of E-2-formylamino-4-phenyl-5-diethylphosphono-3-pentenoic acid methyl ester are dissolved in 10 ml of 4.5N hydrochloric acid and heated at 75° for 192 hours. After concentration in vacuo, the foamy residue is dissolved in a small amount of ethanol and 1 ml of ethanol/propylene oxide (1:1) is added dropwise thereto. The resulting white precipitate is filtered off and recrystallised from water/acetone (1:2). E-2-amino-4-phenyl-5-phosphono-3-pentenoic acid is thus obtained inthe form of colourless needles, m.p. 230°-233°.

후처리

  1. temperatureheated at 75° for 192 hours
  2. concentrationAfter concentration in vacuo
  3. dissolutionthe foamy residue is dissolved in a small amount of ethanol and 1 ml of ethanol/propylene oxide (1:1)
  4. additionis added dropwise
  5. filtrationThe resulting white precipitate is filtered off
  6. customrecrystallised from water/acetone (1:2)

출처 및 근거

ORD 기록
ord-bfb1417611ca46f6a0a1fccc09044fa2
출처 데이터셋
uspto-grants-1991_09
특허 번호
US05051413

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