HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 22758348, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1,3-Propanedithiol | HCID 8013 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 70620281 | HCID 70620281 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 22758348 | HCID 22758348 | — |
Reaction Steps
10 g of 3', 4'-dimethoxy-4-(methylveratrylamino)butyrophenone hydrochloride are dissolved in 50 ml of chloroform and treated with 3.25 g of 1,3-propanedithiol. Hydrogen chloride is conducted into the mixture at room temperature. After standing for 24 hours, the mixture is poured on to water, made basic with 3-N sodium hydroxide and extracted with ether. After drying and evaporation of the solvent, the oily residue is dissolved in acetone and treated with an equivalent amount of anhydrous oxalic acid. The crystalline precipitate is recrystallized from acetone. There is obtained 2-(3,4-dimethoxyphenyl)-N-methyl-N-veratryl-m-dithiane-2-propylamine oxalate (1:1) of melting point 133°-136° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04073797 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-19c6eb7dda1f47fe96f2d130116758c0 |
| Source note | uspto-grants-1978_02 |