تفاعل #84732

ord-077a42d133124a1b9775569963818e3b

معادلة التفاعل

Nc1cc(Cl)c(Br)cc1C(=O)O
2-amino-5-bromo-4-chlorobenzoic acid
[BH4-]
borohydride
Nc1cc(Cl)c(Br)cc1CO
title compound
المردود 71.0%
Nc1cc(Cl)c(Br)cc1CO
(2-amino-5-bromo-4-chlorophenyl)methanol
المردود 71.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction mixture was quenched with methanol (50 mL)
  2. 2
    تركيزconcentrated to a volume of 50 mL
  3. 3
    workup.ADDITIONThe residue was diluted with water (100 mL)
  4. 4
    استخلاصextracted with ethyl acetate (150 mL×3)
  5. 5
    أخرىThe organic layers were separated
  6. 6
    غسيلwashed with water (100 mL) and brine (100 mL)
  7. 7
    تجفيفdried over sodium sulfate
  8. 8
    ترشيحfiltered
  9. 9
    تركيزconcentrated

الإجراء التجريبي

To a solution of 2-amino-5-bromo-4-chlorobenzoic acid (9.0 g, 36.0 mmol) in THF (150 mL) was added borohydride in THF (144 mL, 1 M) at room temperature, and the reaction mixture was stirred overnight. The reaction mixture was quenched with methanol (50 mL), and concentrated to a volume of 50 mL. The residue was diluted with water (100 mL) and extracted with ethyl acetate (150 mL×3). The organic layers were separated, combined, washed with water (100 mL) and brine (100 mL), dried over sodium sulfate, filtered and concentrated to afford the title compound (crude, 6 g, 71%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09434700B2uspto-grants-2016_09