HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 53968269, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2-Chloro-N-methyl-6,7-dihydro-5H-benzo[7]annulen-7-amine--hydrogen chloride (1/1) | HCID 3046878 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 53968269 | HCID 53968269 | 60.9% |
Reaction Steps
7.7 ml of an aqueous solution of 40% formaldehyde and then 4.5 g of sodium cyanoborohydride were added to a mixture of 4.7 g of 2-chloro-7-methylamino-6,7-dihydro [5H] benzocycloheptene hydrochloride in 47 ml of acetonitrile and the mixture was stirred for 15 minutes at room temperature. Acetic acid was added to the reaction mixture until the pH was 7 and the mixture was stirred at room temperature for 45 minutes. The mixture was evaporated to dryness under reduced pressure to obtain 2.6 g of 2-chloro-7-dimethylamino-6,7-dihydro [5H] benzocycloheptene in the form of an oil. Addition of a solution of fumaric acid in methanol yielded 3.3 g of the fumarate of the said product melting at 160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04091115 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-1012aefaa85c4151b8156aba7696ed07 |
| Source note | uspto-grants-1978_05 |