Acetaldehyde → Benzyl-N-(1-cyanoethyl)glycine hydrochloride

HRID 1795792노트

반응식

HRID 1795792 반응식
C[Si]([C:5]#[N:6])(C)C.[CH2:7]([NH:14][CH2:15][C:16]([OH:18])=[O:17])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[CH:19](=O)[CH3:20].[Cl:22]CCl>>[ClH:22].[CH2:7]([N:14]([CH:19]([C:5]#[N:6])[CH3:20])[CH2:15][C:16]([OH:18])=[O:17])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1

참가 물질

5

반응물 4

HCID 177AcetaldehydeHCID 6344DichloromethaneHCID 82115Trimethylsilyl cyanideHCID 869652-(Benzylamino)acetic acid

생성물 1

HCID 68560147Benzyl-N-(1-cyanoethyl)glycine hydrochloride

실험 절차

Trimethylsilyl cyanide (4.0 mL, 30 mmol) was added cautiously to a stirred solution of benzyl glycine free base (5.0 g, 30 mmol) and acetaldehyde (1.7 mL, 30 mmol) in dichloromethane (15 mL) under argon atmosphere. After 15 hours, the volatile components were removed in vacuo, and the residue was dissolved in ethyl acetate (200 mL), washed with brine (100 mL), dried (Na2SO4) and evaporated to an oil. The oil was redissolved in ether (30 mL) and ethanol (30 mL), and 1 M HCl in ether (33 mL) was added dropwise to give the title compound as an off-white crystalline precipitate (6.60 g, 100%). mp: 137–138° C. 1H NMR (CD3OD) δ 7.31–7.48 (m, 5 H), 5.32 (s, 2 H), 4.68 (q, 1 H, J=7.0 Hz), 4.22 (s, 2 H), 1.73 (d, 3 H, J=7.1 Hz). CI MS m/z=192 (M+H). Anal. Calcd. for C12H14N2O2.HCl: C, 56.49; H, 5.95; N, 11.00. Found: C, 56.32; H, 5.88; N, 10.89.

후처리

  1. customthe volatile components were removed in vacuo
  2. dissolutionthe residue was dissolved in ethyl acetate (200 mL)
  3. washwashed with brine (100 mL)
  4. dry with materialdried (Na2SO4)
  5. customevaporated to an oil
  6. dissolutionThe oil was redissolved in ether (30 mL)
  7. additionethanol (30 mL), and 1 M HCl in ether (33 mL) was added dropwise

출처 및 근거

ORD 기록
ord-7b0bb847a4a445d39fa4924d87c6f894
출처 데이터셋
uspto-grants-2006_04
특허 번호
US07030110B2

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