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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055701Generated: November 1, 2026

Acetic Acid → HCID 39235372, compound

https://huagongshe.com/reaction/2055701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetoneHCID 180—
Reactant4-CyanopiperidineHCID 138223—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 39235372HCID 39235372—

Reaction Steps

To a solution of 4-cyanopiperidine (5.8 g, 53 mmol, J. Org. Chem. 21, 984-986, 1957) in methanol (30 mL) and THF (130 mL) was added with stirring acetone (7.7 mL) and glacial acetic acid (6.0 mL) followed by portion wise addition of sodium cyanoborohydride (6.6 g, 105 mmol). When addition was complete the mixture was stirred overnight at ambient temperature. The solvent was evaporated and to the residue was added 1N hydrochloric (110 mL) until pH 1. The mixture was washed with diethyl ether (100 mL) and the acidic aqueous phase was saturated with potassium carbonate. The alkaline mixture (pH 10) was extracted with ethyl acetate (2×200 mL). The combined organic extracts were dried (MgSO4) and the solvent was evaporated. This afforded 8.2 g of 1-isopropyl-4-cyanopiperidine. 1H NMR 400 MHz, DMSO-d6) δ 0.96 (d, 6H), 1.63-1.73 (m, 2H), 1.80-1.92 (m, 2H), 2.35-2.44 (m, 2H), 2.58-2.67 (m, 2H), 2.69-2.78 (m, 1H), 2.79-2.87 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332508B2
Source datasetuspto-grants-2008_02
ORD IDord-6274a45f6c0c4c1b84cefc4d87e741ec
Source noteuspto-grants-2008_02