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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398817Generated: October 26, 2026

1-Aminocyclohexanecarboxylic acid → (1-Aminocyclohexyl)methanol

https://huagongshe.com/reaction/398817

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Aminocyclohexanecarboxylic acidHCID 1366—
ReactantBoron trifluoride etherateHCID 8000—
ReactantSodium HydroxideHCID 14798—
ReactantDiboronHCID 6328200—
SolventTetrahydrofuranHCID 8028—
SolventOxolane--water (1/1)HCID 21881883—
Product(1-Aminocyclohexyl)methanolHCID 40915373.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

1-Amino-1-cyclohexanecarboxylic acid(51.5 g, Aldrich) was added to 150 ml of THF followed by boron trifluoride etherate(27 ml, Aldrich). The reaction mixture was heated to 40° C., stirred for 10 minutes and then a 1.0M solution of diborane(380 ml, Aldrich) was added. The mixture was refluxed for 2 hr, cooled and added THF/water (1:1,25 ml) followed by 6N NaOH(95 ml). The reaction mixture was refluxed for 2 hr, cooled to room temperature and the organic layer was separated, washed with brine, dried and concentrated to give a light yellow oil (34.0 g). 1H NMR consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05817652
Source datasetuspto-grants-1998_10
ORD IDord-c0bd5afdf5d24bb9be41dc17dd574719
Source noteuspto-grants-1998_10