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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369387Generated: October 31, 2026

4-Aminocyclohexanecarboxylic acid → ((1s,4s)-4-Aminocyclohexyl)methanol

https://huagongshe.com/reaction/2369387

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminocyclohexanecarboxylic acidHCID 171560—
ReactantBorane;tetrahydrofuranHCID 2723981—
SolventTetrahydrofuranHCID 8028—
Product((1s,4s)-4-Aminocyclohexyl)methanolHCID 42439078%

Reaction Steps

To a solution of (1r,4r)-4-aminocyclohexanecarboxylic acid (860 mg, 6.0 mmol, 1.0 eq) in THF (10 mL) was added dropwise BH3/THF (1.0 mol/L in THF, 30 mL, 5.0 equiv.) at 0° C. The reaction was allowed to warm to room temperature. The reaction was heated at reflux for 48 hours. The reaction was quenched with AcOH and concentrated in vacuo to get crude ((1r,4r)-4-aminocyclohexyl)methanol (600 mg, 78%) which was used to the next step without further purification. MS: m/z 130.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703941B2
Source datasetuspto-grants-2014_04
ORD IDord-66303fdfd0c64d9dbc2572d8e69ecb95
Source noteuspto-grants-2014_04