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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49714Generated: October 30, 2026

Hydrochloric Acid → (3-Acetoxy-4-nitro-phenyl)acetic acid

https://huagongshe.com/reaction/49714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
Reactant2-(3-Hydroxy-4-nitrophenyl)acetic acidHCID 23508325—
SolventDiethyl EtherHCID 3283—
Product(3-Acetoxy-4-nitro-phenyl)acetic acidHCID 17946639519.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred mixture of (3-hydroxy-4-nitro-phenyl)acetic acid (1 2.0 g), aqueous sodium hydroxide (152.3 mL, 1M) and diethyl ether (150 mL), cooled to 0° C. in an ice salt bath, was treated dropwise with acetic anhydride (8.1 g) at a rate to maintain the temperature at 0° C. When the addition was complete the mixture was stirred at 0° C. for a further 2 hours then acidified with dilute hydrochloric acid and then extracted with ethyl acetate. The extracts were dried over magnesium sulphate and then evaporated to give the title compound (12.6 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706738B2
Source datasetuspto-grants-2004_03
ORD IDord-60d046c6b3554acfb33ad147ac87161e
Source noteuspto-grants-2004_03