HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 10521715, compound → HCID 10617602, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 10521715 | HCID 10521715 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 10617602 | HCID 10617602 | — |
Reaction Steps
28.82 g (0.083 mol) of 3-(1-methylcyclohexyl)-4-tert-butyldimethylsilyloxybenzoic acid, in 300 ml ether, are treated at -20° C. under nitrogen, with 0.166 mol of methyllithium (1.6M in ether). The reaction mixture is stirred under nitrogen overnight and it is then treated as for Example 25(a). After filtration of the residue on silica, 22 g (76%) of the expected product are isolated in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05547983 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-c5348c917f55474f9c03355d820d6878 |
| Source note | uspto-grants-1996_08 |