Reaktion #559282

ord-a1c9003ad8b345079e2a1b6e16d12676

Reaktionsgleichung

CC(=O)O
acetic acid
[Na+].[OH-]
NaOH
O=C(Cl)OCc1ccccc1
benzyl chloroformate
Cc1cc(C(=O)O)ccc1N
4-amino-3-methylbenzoic acid
Cc1cc(C(=O)O)ccc1NC(=O)OCc1ccccc1
title compound
Ausbeute 68.1%
Cc1cc(C(=O)O)ccc1NC(=O)OCc1ccccc1
4-Benzyloxycarbonylamino-3-methyl-benzoic acid
Ausbeute 68.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationthe solids collected by filtration
  2. 2
    WaschenThe filter cake was rinsed with water
  3. 3
    WaschenThe organic was washed with brine
  4. 4
    Trocknendried over MgSO4
  5. 5
    Filtrationfiltered
  6. 6
    Einengenconcentrated
  7. 7
    SonstigeThe resulting solid was dried under vacuum

Vorschrift

A mixture of 4-amino-3-methylbenzoic acid (35.1 g, 232 mmol) in water (400 mL) was treated with 2.5N NaOH (200 mL, 500 mmol) and benzyl chloroformate (37.0 mL, 259 mmol). After 1 h, 150 mL water was added, the resulting mixture was treated with glacial acetic acid (15 mL) and the solids collected by filtration. The filter cake was rinsed with water and the resulting solid taken up in ethyl acetate/2-methyl tetrahydrofuran. The organic was washed with brine, dried over MgSO4, filtered and concentrated. The resulting solid was dried under vacuum to give 45.1 g of the title compound. LCMS m/z=307.9 MH+, Rt=2.508 min.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08633206B2uspto-grants-2014_01