HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21895Generated: October 26, 2026
Sulfuric Acid → trans-Ethyl 2-hydroxycyclohexanecarboxylate
https://huagongshe.com/reaction/21895
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ethyl 2-oxocyclohexanecarboxylate | HCID 95543 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | trans-Ethyl 2-hydroxycyclohexanecarboxylate | HCID 1268212 | 11.6% |
Reaction Steps
Ethyl cyclohexanone-2-carboxylate (85.0 g, 0.5 mole) was dissolved in ethanol (200 ml) and the solution cooled to 0° C. Sodium borohydride (13.2 g, 0.35 mole) suspended in ethanol (80 ml) was added in small portions whilst the temperature was maintained at below 0° C. After stirring for 2 hours at 0° C. the reaction mixture was made faintly acid by the addition of 50% sulphuric acid and filtered. The filtrate was concentrated in vacuo, taken up in ether and washed with sodium bicarbonate solution. The organic phase was dried over magnesium sulphate and evaporated in vacuo. The residue was chromatographed on silica-gel, eluting initially with 3:1 hexane/ethyl acetate followed by 2:1 hexane/ethyl acetate to give 21.5 g of cis- and 10.0 g of trans-ethyl 2-hydroxycyclohexanecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05426090 |
|---|
| Source dataset | uspto-grants-1995_06 |
|---|
| ORD ID | ord-5cebf6cc66d246d19ec89f9f74c35655 |
|---|
| Source note | uspto-grants-1995_06 |
|---|