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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451633Generated: October 31, 2026

(4-Nitrophenoxy)acetic acid → (4-Nitrophenoxy)acetyl chloride

https://huagongshe.com/reaction/1451633

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Nitrophenoxy)acetic acidHCID 15720—
ReactantThionyl ChlorideHCID 24386—
Product(4-Nitrophenoxy)acetyl chlorideHCID 88380—

Reaction Steps

A mixture of (4-nitrophenoxy)acetic acid (50 g) and thionyl chloride (150 ml) was heated under reflux for 3 h. The solution was concentrated and then coevaporated with benzene to give 4-nitrophenoxyacetyl chloride as a solid. A solution of this solid (9.4 g) in acetone (100 ml) was added dropwise to a stirred mixture of 1,2,3,4-tetrahydro-6,7-dimethoxyisoquinoline hydrochloride (10 g) and sodium hydrogen carbonate (9 g) in acetone (100 ml) at 0°. Stirring was continued at room temperature for 16 h, the mixture was then filtered, and the filtrate was concentrated. The residue was treated with water and extracted with dichloromethane. The organic layer was washed with water, dried and concentrated to give the title compound (6.6 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604237
Source datasetuspto-grants-1997_02
ORD IDord-e52edaf67e604cc1bdcca2088a6272d6
Source noteuspto-grants-1997_02