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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247176Generated: November 1, 2026

Chloride → 2H-1,2-Benzoxazin-3(4H)-one

https://huagongshe.com/reaction/1247176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantTerephthalic AcidHCID 7489—
ReactantTriethylamineHCID 8471—
CatalystDimethylformamideHCID 6228—
Product2H-1,2-Benzoxazin-3(4H)-oneHCID 1993744866%

Reaction Steps

Into 50 mL methylene chloride was dissolved 0.682 g (2 mmol) of the above intermediate terephthalic acid, followed by 5 drops DMF and 3.88 mL (48 mmol) triethylamine. The mixture was cooled in an ice bath, and 0.42 mL (4.8 mmol) oxayl chloride was added in one portion. After 30 min 10 mL MeOH was added and ice bath was removed. After stirring an additional 30 min, the mixture was shaken between EtOAc (100 mL) and cold dilute HCl (100 mL). The organic layer was washed with satd NaHCO3 (100 mL), dried (MgSO4), and evaporated. Crystalline desired benzoxazinone (456 g, 66%) was obtained from a concentrated methylene chloride-hexane solution.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129245B2
Source datasetuspto-grants-2006_10
ORD IDord-bf5352a747634a1ba543ee5e8c0b8564
Source noteuspto-grants-2006_10