تفاعل #1772021

ord-0fcbaaba3fb7440185b5d72e6e387a3c

معادلة التفاعل

CCN=C=NCCCN(C)C
EDCI
O=C(O)C(Br)c1ccccc1
α-bromophenylacetic acid
C[C@H](O)c1ccccc1
(S)-(−)-1-phenylethanol
C[C@H](OC(=O)C(Br)c1ccccc1)c1ccccc1
title compound
المردود 73.0%
C[C@H](OC(=O)C(Br)c1ccccc1)c1ccccc1
(S)-1-Phenylethyl 2-bromo-2-phenylacetate
المردود 73.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلwashed (H2O×2, brine)
  2. 2
    تجفيفdried (Na2SO4)
  3. 3
    ترشيحfiltered
  4. 4
    تركيزconcentrated
  5. 5
    أخرىto give a pale yellow oil

الإجراء التجريبي

To a mixture of α-bromophenylacetic acid (10.75 g, 0.050 mol), (S)-(−)-1-phenylethanol (7.94 g, 0.065 mol) and DMAP (0.61 g, 5.0 mmol) in dry dichloromethane (100 mL) was added solid EDCI (12.46 g, 0.065 mol) all at once. The resulting solution was stirred at room temperature under Ar for 18 hours and then it was diluted with ethyl acetate, washed (H2O×2, brine), dried (Na2SO4), filtered, and concentrated to give a pale yellow oil. Flash chromatography (SiO2/hexane-ethyl acetate, 4:1) of this oil provided the title compound (11.64 g, 73%) as a white solid. 1H NMR (400 MHz, CDCl3) δ 7.53-7.17 (m, 10H), 5.95 (q, J=6.6 Hz, 0.5H), 5.94 (q, J=6.6 Hz, 0.5H), 5.41 (s, 0.5H), 5.39 (s, 0.5H), 1.58 (d, J=6.6 Hz, 1.5H), 1.51 (d, J=6.6 Hz, 1.5H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08147818B2uspto-grants-2012_04