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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058996Generated: November 2, 2026

Acetyl bromide → HCID 12833523, compound

https://huagongshe.com/reaction/2058996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl bromideHCID 10482—
ReactantFenoldopam monohydrobromideHCID 11957552—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 12833523HCID 12833523—

Reaction Steps

6-Chloro-7,8-dihydroxy-1-p-hydroxyphenyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrobromide (Example 2, 1.0 g) was slurried in 200 ml of trifluoroacetic acid then 1.29 ml of acetyl bromide was added. The mixture was heated at reflux for 2 hours then stirred for 2 hours. After evaporation to dryness the residue was taken up in benzene and concentrated to give a solid which was recrystallized from ethylacetatehexane to give 6-chloro-7,8-diacetoxy-1-(p-acetoxyphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine hydrobromide; m.p. 214.5°-217°, 0.77 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04321195
Source datasetuspto-grants-1982_03
ORD IDord-93e01013a1a94587a9d8702adc8f09b9
Source noteuspto-grants-1982_03