HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl bromide → HCID 20531692, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | HCID 20531683 | HCID 20531683 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 20531692 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04340600 |
| Source dataset | uspto-grants-1982_07 |
| ORD ID | ord-6f494e64ba7a48d7804e9937f1de5768 |
| Source note | uspto-grants-1982_07 |