HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → trans-4-Hydroxycyclohexane-1-carboxylic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Hydroxycyclohexanecarboxylic acid | HCID 151138 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | trans-4-Hydroxycyclohexane-1-carboxylic acid benzyl ester | HCID 14296103 | — |
Reaction Steps
To a solution of 4-hydroxycyclohexane carboxylic acid (19.95 g, 138.4 mmol) in 100 mL of degassed DMF was added potassium carbonate (21.0 g, 152.2 mmol) and benzyl bromide (15.61 mL, 131.4 mmol). After 16 hours at room temperature, the reaction mixture was poured into 500 mL of water and extracted 3 times with EtOAc. The combined organic layers were washed with water and brine prior to drying over sodium sulfate. Filtration and solvent removal provided benzyl 4-hydroxycyclohexane carboxylate as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07816380B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-01a4462491914b17b2aa8ddf13e7c84b |
| Source note | uspto-grants-2010_10 |