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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759321Generated: October 30, 2026

Acetyl bromide → HCID 20531692, compound

https://huagongshe.com/reaction/1759321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl bromideHCID 10482—
ReactantHCID 20531683HCID 20531683—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 20531692HCID 20531692—

Reaction Steps

A mixture of 1.0 g of 8-hydroxy-1-(3,4-dihydroxyphenyl)-2-methyl-1,2,3,4-tetrahydroisoquinoline hydrobromide prepared as in Example 4 above and 200 ml of trifluoroacetic acid is mixed with 1.3 ml of acetyl bromide. After heating at reflux for 2 hours, the mixture is evaporated to dryness. The residue is purified by recrystallization to give 8-acetoxy-1-(3,4-diacetoxyphenyl)-2-methyl-1,2,3,4-tetrahydroisoquinoline hydrobromide. Similarly isobutyryloxy, propionyloxy, isovaleryloxy, n-butylryloxy and n-heptanoyloxy derivatives are prepared.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04340600
Source datasetuspto-grants-1982_07
ORD IDord-6f494e64ba7a48d7804e9937f1de5768
Source noteuspto-grants-1982_07