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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231046Generated: October 27, 2026

Methyl chloroformate → 4-chloro-3-isobutyryloxy-10H-phenothiazine

https://huagongshe.com/reaction/231046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantIsobutyric AcidHCID 6590—
ReactantTriethylamineHCID 8471—
Reactant4-chloro-3-hydroxy-10H-phenothiazineHCID 9881418—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-chloro-3-isobutyryloxy-10H-phenothiazineHCID 13882030—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of iso-butyric acid (1.6 ml) in THF (10 ml) at 0° C. was added Et3N (2.7 ml) and methylchloroformate (1.5 ml). To this resulting suspension was added slowly at 0° C. a solution of 4-chloro-3-hydroxy-10H-phenothiazine in THF (10 ml). The reaction mixture was stirred at 5° C. for 12 hours, after which H2O was added and the resulting aqueous phase extracted with ethyl acetate. The organic layer was then dried and evaporated. The resulting residue was purified by chromatography on silica gel to give 2.25 g of 4-chloro-3-isobutyryloxy-10H-phenothiazine (m.p. 155° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04845083
Source datasetuspto-grants-1989_07
ORD IDord-4eee8099bf5e42adb2288e40d48a137f
Source noteuspto-grants-1989_07