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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109821Generated: October 23, 2026

Hydrochloric Acid → 4-Chloro-3,6-dihydrophthalic anhydride

https://huagongshe.com/en/reaction/1109821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloropreneHCID 31369—
ReactantChloromaleic anhydrideHCID 66772—
ReactantDichloromaleic anhydrideHCID 70728—
CatalystPhenothiazineHCID 7108—
SolventWaterHCID 962—
SolventChlorobenzeneHCID 7964—
Product4-Chloro-3,6-dihydrophthalic anhydrideHCID 10986977498.4%

Reaction Conditions

Temperature92 °C

Reaction Steps

A 3-necked 50 mL flask was equipped with a pressure equalizing additional funnel, a thermocouple well with a thermocouple, a water cooled condensor and a magnetic stir bar. The flask was charged with 6.62 g (0.05 mol) of monochloromaleic anhydride contaminated with approximately 0.005 mol of dichloromaleic anhydride, 6.1 g of monochlorobenzene and 100 mg of phenothiazine. The contents of the flask were heated to 92° C. and 4.42 g (0.05 mol) of chloroprene was added over 15 to 30 minutes. HCl gas was observed evolving from the reactor. After 16 hours at 92° C., the solvent was removed in-vacuo and triturated with 10 mL of diethyl ether to yield 4.6 g (50% of theoretical) of 4-chloro-3,6-dihydrophthalic anhydride. High resolution mass spectrometry (MS) of the solid resulted in the following analysis: Calculated mass=183.99271; observed mass=183.9924. 13C and 1H nuclear magnetic resonance (NMR) spectra were consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05322954
Source datasetuspto-grants-1994_06
ORD IDord-4a0b8bc91ed94c54b4a3af367b25209d
Source noteuspto-grants-1994_06