تفاعل #3059

ord-31db870c320a495ea81c261721daf508

معادلة التفاعل

Cl.NOCc1ccccc1
O-benzylhydroxylamine hydrochloride
O=C(Br)CBr
bromoacetyl bromide
CCN(C(C)C)C(C)C
diisopropylethylamine
O=C(CBr)NOCc1ccccc1
title compound
المردود 52.0%
O=C(CBr)NOCc1ccccc1
Bromo-N-(benzyloxyl)acetamide
المردود 52.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe aqueous layer was separated
  2. 2
    استخلاصextracted with ethyl acetate
  3. 3
    تجفيفdried over Na2SO4
  4. 4
    ترشيحfiltered
  5. 5
    تركيزconcentrated in vacuo
  6. 6
    أخرىThe crude material was purified by silica gel flash column chromatography with ethyl acetate-hexane

الإجراء التجريبي

To a 0° C. solution of O-benzylhydroxylamine hydrochloride (1.6 g, 10 mmol) in THF (40 mL) was added bromoacetyl bromide (871 μL, 10 mmol) and diisopropylethylamine (3.5 mL, 20 mmol). The reaction mixture was warmed to room temperature overnight and diluted with ethyl acetate and water. The aqueous layer was separated and extracted with ethyl acetate. The organic layers were combined, dried over Na2SO4, filtered and concentrated in vacuo. The crude material was purified by silica gel flash column chromatography with ethyl acetate-hexane to give 1.27 g (52%) of the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05731438uspto-grants-1998_03