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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759315Generated: November 2, 2026

Acetyl bromide → HCID 20531733, compound

https://huagongshe.com/reaction/1759315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl bromideHCID 10482—
ReactantHCID 20531732HCID 20531732—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 20531733HCID 20531733—

Reaction Steps

A mixture of 1 g of 2-allyl-8-chloro-6,7-dihydroxy-4-(p-hydroxyphenyl)-1,2,3,4-tetrahydroisoquinoline hydrobromide, 1.3 ml of acetyl bromide and 200 ml of trifluoroacetic acid is stirred at 10° for 2 hours. After evaporation to dryness, the residue is purified, if necessary, by recrystallization to give 2-allyl-8-chloro-6,7-diacetoxy-4-(p-acetoxyphenyl)-1,2,3,4-tetrahydroisoquinoline hydrobromide. Similarly tri-isobutyryloxy, -propionyloxy, -isovaleryloxy, -n-butyryloxy and -n-heptanoyloxy ester derivatives are prepared.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04340601
Source datasetuspto-grants-1982_07
ORD IDord-328e998392cb4e92809fa239a8d20fcc
Source noteuspto-grants-1982_07