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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261137Generated: November 3, 2026

HCID 22394176, compound → HCID 23349430, compound

https://huagongshe.com/reaction/261137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22394176HCID 22394176—
ReactantHCID 86736609HCID 86736609—
SolventBenzeneHCID 241—
ProductHCID 23349430HCID 23349430—

Reaction Steps

6.32 g of 2-bromomethyl-5-chloroaniline hydrobromide is added to 30 ml of benzene containing 12.5% phosgene (w/v) and the mixture refluxed in a vessel equipped with a Dean-Stark trap and additional phosgene/benzene added for a total of 250 ml (over a period of 6 hrs; 1/2 ml of water collected in the trap). The reaction mixture is cooled to 20°, insolubles removed by filtration and the filtrate concentrated (solvent removed), then distilled under vacuum to obtain 2-bromomethyl-5-chlorophenylisocyanate (distills at 0.05 mm Hg/50°). Further distillation yields 2-bromomethyl 4-bromo-5-chlorophenyl isocyanate (which may be refined by crystallization from petroleum ether, m.p. 48°-50°) which is useful as an intermediate in Examples 4 and 5 in preparing 6-bromo-7-chloro-4H-1,3-benzoxazine analogs of the title product of this example.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04164407
Source datasetuspto-grants-1979_08
ORD IDord-5fde71c3705f4d8f94d4e51f2a84bf80
Source noteuspto-grants-1979_08