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Potassium thiocyanate → (-)-alpha-Amino-3-(thiocyanatomethyl)-4-hydroxybenzeneacetic acid

HRID 903826
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HRID 903826 반응식
[NH2:1][CH:2]([C:6]1[CH:11]=[CH:10][C:9]([OH:12])=[C:8]([CH2:13]Cl)[CH:7]=1)[C:3]([OH:5])=[O:4].[S-:15][C:16]#[N:17].[K+]>CO>[NH2:1][CH:2]([C:6]1[CH:11]=[CH:10][C:9]([OH:12])=[C:8]([CH2:13][S:15][C:16]#[N:17])[CH:7]=1)[C:3]([OH:5])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 516872Potassium thiocyanateHCID 20296136(-)-alpha-Amino-3-(chloromethyl)-4-hydroxybenzeneacetic acid

생성물 1

HCID 23329809(-)-alpha-Amino-3-(thiocyanatomethyl)-4-hydroxybenzeneacetic acid수율 78%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of (-)-α-amino-3-(chloromethyl)-4-hydroxybenzeneacetic acid (0.5 g, 1.98 mmole) and potassium thiocyanate (0.4 g, 4.12 mmole) in 10 ml of methanol is stirred at room temperature for 16 hours. The reaction mixture is filtered to remove the potassium chloride, the filtrate is evaporated and to the residue is added saturated aqueous sodium bicarbonate until the pH is 7. The title compound precipitates as a white powder which is filtered and dried. (1.83 g, 78% yield), NMR (TFA-D+D2O) ppm (δ) 4.1 (s,2), 5.08 (s,1), 6.9-7.3 (m,3).

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후처리

  1. filtrationThe reaction mixture is filtered
  2. customto remove the potassium chloride
  3. customthe filtrate is evaporated and to the residue
  4. additionis added saturated aqueous sodium bicarbonate until the pH is 7
  5. customThe title compound precipitates as a white powder which
  6. filtrationis filtered
  7. customdried

출처 및 근거

ORD 기록
ord-95b6e6a13b034569841168dbca03942c
출처 데이터셋
uspto-grants-1980_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04229363

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