HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → [1-(2-Hydroxy-ethyl)-cyclohexyl]-acetic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | (1-Benzyloxycarbonylmethyl-cyclohexyl)-acetic acid | HCID 14036669 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [1-(2-Hydroxy-ethyl)-cyclohexyl]-acetic acid benzyl ester | HCID 66675168 | 79.6% |
Reaction Steps
A solution of (1-benzyloxycarbonylmethyl-cyclohexyl)-acetic acid (3.0 g, 10 mmol) in tetrahydrofuran (20 mL) was cooled to 0° C. and 1 M borane-THF complex in tetrahydrofuran (21 mL, 20 mmol) was added dropwise over 5 min. The reaction mixture was allowed to warm to room temperature, stirred for 1 h at room temperature. and cooled to 0° C. Methanol was added slowly to quench the reaction. The reaction mixture was warmed to room temperature, stirred for 30 min, and concentrated to dryness to provide the title compound (2.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08314128B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-5fdd5eafbe444fc1aeef0dda365744ae |
| Source note | uspto-grants-2012_11 |