反应 #1702029

ord-881ffdc9cc164be399ef28c962fe846d

反应方程式

O=C(O)CNc1ccc(O)cc1
N-(4-hydroxyphenyl)glycine
O=C(Cl)OCc1ccccc1
Benzyl chloroformate
O
water
O=C(O)CN(C(=O)OCc1ccccc1)c1ccc(O)cc1
2-((benzyloxycarbonyl)(4-hydroxyphenyl)amino)acetic acid
收率 75.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGstirred at ambient conditions for 18 h
  2. 2
    workup.WAITstored at 4° C. for 24 h
  3. 3
    其他The product was isolated
  4. 4
    其他recrystallized in warm ethanol
  5. 5
    其他dried in vacuum oven at 40° C. overnight (yield 75%, mp=196-198° C.)

实验过程

N-(4-hydroxyphenyl)glycine (55.0 g, 0.330 mol) was dissolved in 275 mL of N-methylpyrrolidone in a 1 L round-bottomed flask. Benzyl chloroformate (50.1 mL, 0.352 mol) was added with stirring over a 40 min period and then stirred at ambient conditions for 18 h. Deionized water was added until slightly turbid and then stored at 4° C. for 24 h. The product was isolated and recrystallized in warm ethanol, dried in vacuum oven at 40° C. overnight (yield 75%, mp=196-198° C.). 1H-NMR (500 MHz, DMSO-d6) δ 12.80 (s, 1H, COOH), 9.50 (s, 1H, phenol), 7.58-6.95 (m, 7H, aryl), 6.74 (s, 2H, aryl), 5.10 (d, J=21.9, 2H, —CH2-benzyl), 4.22 (d, J=21.7, 2H, N—CH2-).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08765161B2uspto-grants-2014_07