HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505274Generated: October 30, 2026
HCID 178471800, compound → HCID 178471796, compound
https://huagongshe.com/reaction/505274
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 178471800 | HCID 178471800 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178471796 | HCID 178471796 | — |
Reaction Steps
To a solution of trans-4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid (385.6 mg, 1.80 mmol) in THF (20 mL) was added BH3 (2.7 mL of a 1M solution in THF, 2.70 mmol). After 2 hours, the reaction was quenched by careful addition of H2O (10 mL). The mixture was extracted with EtOAc (80 mL) and the organic layer was washed with water and brine (20 mL each). The organic layer was dried over Na2SO4, filtered, and concentrated. Purification of the residue by flash chromatography on silica gel (5 to 60% EtOAc/hexanes) afforded ethyl [trans-4-(hydroxymethyl)cyclohexyl]acetate. Rf=0.26 (40% EtOAc/hexanes). 1H NMR (CDCl3, 600 MHz) δ 4.12 (q, J=7.1 Hz, 2H), 3.45 (d, J=6.5 Hz, 2H), 2.19 (d, J=7.0 Hz, 2H), 1.72-1.82 (m, 5H), 1.45 (m, 1H), 1.25 (t, J=7.1 Hz, 3H), 0.96-1.05 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781426B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-623152c8758a445f868eca0648c78895 |
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| Source note | uspto-grants-2010_08 |
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