HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl bromide → HCID 20531733, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | HCID 20531732 | HCID 20531732 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 20531733 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04340601 |
| Source dataset | uspto-grants-1982_07 |
| ORD ID | ord-328e998392cb4e92809fa239a8d20fcc |
| Source note | uspto-grants-1982_07 |