HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Naphthoic acid → 1,2,3,4-Tetrahydro-2-naphthoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Naphthoic acid | HCID 7123 | — |
| Reactant | Ethylene glycol diethyl ether | HCID 12375 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Product | 1,2,3,4-Tetrahydro-2-naphthoic acid | HCID 101370 | — |
Reaction Steps
The thus obtained 6-[4'-alkoxy-4-biphenyl)ethyl]-2-naphthalenecarboxylic acid (22) is hydrogenated in the presence of metal sodium in a solvent such as 1,2-diethoxyethane to obtain 6-[4'-alkoxy-4-biphenyl)ethyl]-1,2,3,4-tetrahydro-2-naphthalenecarboxylic acid (23). Finally, the resulting 6-[4'-alkoxy-4-biphenyl)ethyl]-1,2,3,4-tetrahydro-2-naphthalenecarboxylic acid (23) is reacted with an alcohol (24) having an asymmetric carbon in the presence of 4-N,N-dimethylaminoprydine, whereby the above-mentioned carboxylate compound (25) represented by the formula (II), in which x is --CH2CH2 --, may be obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05725798 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-bf36940ac45c47b1a49e30e635325cb5 |
| Source note | uspto-grants-1998_03 |