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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296305Generated: November 1, 2026

Ethyl bromoacetate → 8-Chloro-6-phenyl-2H,4H-pyrrolo[3,4-d][2]benzazepine-2-acetic acid ethyl ester

https://huagongshe.com/reaction/2296305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant8-Chloro-6-phenyl-2H,4H-pyrrolo[3,4-d][2]benzazepineHCID 136087684—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product8-Chloro-6-phenyl-2H,4H-pyrrolo[3,4-d][2]benzazepine-2-acetic acid ethyl esterHCID 13067100—

Reaction Steps

To a solution of 1.4 g (12.4 mmole) of potassium t-butoxide in 30 ml of dry dimethylformamide was added 2.4 g (8.2 mmole) of 8-chloro-6-phenyl-2H,4H-pyrrolo[3,4-d][2]benzazepine. The mixture was cooled to 0°, and stirred for 10 min. To the mixture was added 1.3 mol (11.7 mmole) of ethyl bromoacetate. The mixture was stirred at 0° for 45 min, diluted with water, and extracted with ether. The ether solution was washed with water, dried with sodium sulfate, and concentrated at reduced pressure to give a yellow oil. Purification by column chromatography (70 g SiO2, 9:1 methylene chloride/ether) gave as the first major component a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04428879
Source datasetuspto-grants-1984_01
ORD IDord-1b07a4f0c3d94b639b0f7b584f51fa67
Source noteuspto-grants-1984_01