HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 131710681, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetylene | HCID 6326 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | HCID 53902899 | HCID 53902899 | — |
| Reactant | HCID 86734546 | HCID 86734546 | — |
| Product | HCID 131710681 | HCID 131710681 | — |
Reaction Steps
In a manner similar to the method described in example 47, 4.5 g of 6-(p-methoxybenzyl)-7-methyl-7-azaspiro [4.5] decan-10-one (obtained from 8 g of the picrate described in example 36) is reacted with acetylene lithium, prepared by dissolution of 1.1 g of lithium in 200 ml of liquid ammonia saturated with acetylene. The crude reaction product, 10-ethinyl-6-(p-methoxybenzyl)-7-methyl-7-azaspiro [4.5] decan-10-ol, is submitted to catalytic hydrogenation in the usual manner, giving the above-mentioned compound. The hydrochloride melts at 217°-220° C with decomposition. Yield 76%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04012392 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-5a648360ff3549e2bd697615a952fa7b |
| Source note | uspto-grants-1977_03 |