HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isoquinoline → 1,2,3,4-Tetrahydroisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isoquinoline | HCID 8405 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | 1,2,3,4-Tetrahydroisoquinoline | HCID 7046 | 88.9% |
Reaction Steps
In an autoclave, 1.2 kg of the same crude isoquinoline as used in Example 2 and 180 g of the aforementioned stabilized nickel catalyst were subjected to hydrogenation at a temperature of 180° C. under a hydrogen pressure of 135 kg/cm2 ·G for 65 hours. The amount of hydrogen absorbed was 29.9 moles and the molar ratio of the hydrogen absorption (by molar ratio based on raw material) was 3.22. The resultant reaction mixture was separated by filtration and then distilled. Consequently, 1.1 kg of 1,2,3,4-tetrahydroisoquinoline (purity 94.6% and total sulfur content 0%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04656279 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-7d2fcae834414187ba19235ee2420fe2 |
| Source note | uspto-grants-1987_04 |