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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975671Generated: October 26, 2026

Hydrochloric Acid → 8-chloro-10,11-dihydro-10-[(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)acetyl]dibenz[b,f][1,4]oxazepine

https://huagongshe.com/reaction/1975671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant2H-Isoindole-2-acetyl chloride, 1,3-dihydro-1,3-dioxo-HCID 81242—
Reactant8-Chloro-10,11-dihydrodibenzo[b,f][1,4]oxazepineHCID 15229227—
SolventTolueneHCID 1140—
Product8-chloro-10,11-dihydro-10-[(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)acetyl]dibenz[b,f][1,4]oxazepineHCID 10669729—

Reaction Steps

1,3-dihydro-1,3-dioxo-2H-isoindole-2-acetyl chloride (4.00 grams), 8-chloro-10,11-dihydrodibenz[b,f][1,4]oxazepine (4.16 grams) and triethylamine (2.8 mi) were refluxed in toluene (100 mi) under nitrogen for 3 hours. The resulting mixture was poured into 1N HCl at 0° C., and the biphasic mixture was shaken vigorously. The insoluble product was collected by filtration, washed with toluene and ethyl ether, and dried in vacuo at 56° C. The yield of the title compound was 6.36 grams (85%). Mp: 184°-185° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05288719
Source datasetuspto-grants-1994_02
ORD IDord-4ff71354d001487c849678e0720ee807
Source noteuspto-grants-1994_02