Ethyl orthoformate → 1,3-Benzoxazole-4-carboxylic acid

HRID 1987986Notes

Reaction equation

HRID 1987986 reaction equation
Br.[NH2:2][C:3]1[C:11]([OH:12])=[CH:10][CH:9]=[CH:8][C:4]=1[C:5]([OH:7])=[O:6].[CH:13](OCC)(OCC)OCC.C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1>>[O:12]1[C:11]2=[CH:10][CH:9]=[CH:8][C:4]([C:5]([OH:7])=[O:6])=[C:3]2[N:2]=[CH:13]1

Participants

4

Reactant 3

HCID 31214Ethyl orthoformateHCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 668807402-Amino-3-hydroxybenzoic acid hydrobromide

Product 1

HCID 183546021,3-Benzoxazole-4-carboxylic acidYield 100.6%

Procedure

A mixture of 2-amino-3-hydroxybenzoic acid hydrobromide (300 mg, 1.28 mmol), triethyl orthoformate (0.85 mL, 5.1 mmol), pyridinium p-toluenesulfonate (64 mg, 0.26 mmol) and xylenes (15 mL) was refluxed for 4 h. The reaction mixture was cooled to room temperature and concentrated under reduced pressure to afford the benzoxazole-4-carboxylic acid (210 mg, quantitative) as a light yellow solid: 1H NMR (300 MHz, DMSO-d6) δ 13.12 (s, 1H), 8.86 (s, 1H), 8.03 (dd, J=8.1, 0.9 Hz, 1H), 7.92 (dd, J=8.1, 0.9 Hz, 1H), 7.54 (t, J=8.1 Hz, 1H); MS (ESI+) m/z 164 (M+H).

Workup

  1. temperaturewas refluxed for 4 h
  2. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-17fabf337a1749818dd3c28a1146078f
Source dataset
uspto-grants-2009_06
Patent number
US07553846B2

Reaction notes

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