HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 12838038, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 8-Chloro-1,2,3,4-tetrahydroisoquinoline--hydrogen chloride (1/1) | HCID 12595072 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12838038 | HCID 12838038 | — |
Reaction Steps
To a mixture of 28.6 g of 8-chloro-1,2,3,4-tetrahydoisoquinoline hydrochloride in 140 ml of dichloromethane was added 140 ml of 1N aqueous NaOH solution and 17.6 g of NaHCO3. To the solution was added dropwise 14.5 ml of acetic anhydride at 5° C. The mixture was stirred at room temperature for 1 hour. The organic layer was separated and the aqueous layer was extracted with dichloromethane. The combined organic extracts were washed with water, dried over anhydrous sodium sulfate. The solvent was distilled off to give 29.1 g of the title compound as a pale red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05273974 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-95ad5da48c2b4f3eac985c169b57df40 |
| Source note | uspto-grants-1993_12 |