HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Dicyclohexylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 86737592 | HCID 86737592 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Dicyclohexylamine | HCID 7582 | 74.7% |
Reaction Steps
1.4 g of 2-(3-benzoylthio-propionyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid dicyclohexylamine salt are dissolved in 20 ml of methanol, and 20 ml of 8 % aqueous ammonia are added thereto. The mixture is stirred at room temperature overnight in nitrogen gas atmosphere. The reaction mixture is condensed to dryness under reduced pressure, and the residue is washed with ether. 0.85 g of 2-(3-mercaptopropionyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid.dicyclohexylamine salt is thereby obtained. Yield: 74.7 % M.p. 193°-194° C.(decomp.) (This product begins to gradually decompose at 176° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04256751 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-af5c46a9bb91446588035dedaca49ccf |
| Source note | uspto-grants-1981_03 |