HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 12928524, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 12928521 | HCID 12928521 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 12928524 | HCID 12928524 | — |
Reaction Steps
Reflux for 4 hours, a solution of 52.0 g (0.18 moles) of the product of step C in a mixture of 96 ml of 37% formaldehyde and 144 ml of 90% formic acid. Distill almost to dryness at 100° C. under reduced pressure (about 100 mm). Dissolve the residue in a mixture of 500 ml of 1 N sodium hydroxide and 500 ml of ethyl ether with cooling and stirring. Separate the ether layer, dry over anhydrous sodium sulfate, and evaporate to give (S)-7-chloro-8-methoxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine as a colorless solid. Obtain an analytically pure sample by crystallization from ethyl ether, m.p. 91°-92° C. [α]D26 =+47.3° (c=1, ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04284555 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-a646f7aa4dcb45a4ad039a2e9e473e49 |
| Source note | uspto-grants-1981_08 |