HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-Chlorophenyl)cyclohexane-1-carboxylic acid → [Trans-4-(4-chlorophenyl)cyclohexyl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-Chlorophenyl)cyclohexane-1-carboxylic acid | HCID 2735792 | — |
| Solvent | Water | HCID 962 | — |
| Product | [Trans-4-(4-chlorophenyl)cyclohexyl]methanol | HCID 53925853 | 64% |
Reaction Steps
4-(4-Chlorophenyl)cyclohexane carboxylic acid (0.35 g, 1.5 mmol) was reacted via Method E over 72 hours. The solid was poured into a water (40 mL) solution and extracted with ethyl acetate (EtOAc) (4×10 mL). The combined organic layers were washed with brine (40 mL) and dried over anhydrous Na2SO4. The organic layer was concentrated in vacuo to obtain [4-(4-chlorophenyl)cyclohexyl]methanol (0.210 g, 64% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07985755B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-d161dfce120c4e5d8e678822da9c3586 |
| Source note | uspto-grants-2011_07 |