Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373174Generated: October 31, 2026

Acetic Anhydride → HCID 58780900, compound

https://huagongshe.com/reaction/1373174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 58780925HCID 58780925—
SolventAcetic AcidHCID 176—
ProductHCID 58780900HCID 58780900—

Reaction Conditions

Temperature50 °C

Reaction Steps

3-Hydroxy-5-(2-methylbenzyloxy) benzoic acid (20.30 g, 78.6 mM) and acetic anhydride (125 ml, 1.32M) in acetic acid (125 ml) were refluxed for 16 hours. The reaction was cooled and the solvent evaporated ‘in vacuo’. Acetic acid (125 nml) and water (125 ml) were added to the resulting residue and the mixture was stirred for 1 hour at 50° C. Toluene (100 ml) was added and the solvent distilled off ‘in vacuo’ to give 3-acetoxy-5-(2-methylbenzyloxy) benzoic acid as a colourless solid (23.6 g); H1 NMR δ (d6-DMSO) 2.25 (3H s) 2.32 (3H s) 5.12 (2H s) 7.09–7.25 (7H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160906B2
Source datasetuspto-grants-2007_01
ORD IDord-bdb1efd5f3b14de8a0d00d011265b3f4
Source noteuspto-grants-2007_01