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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404100Generated: November 2, 2026

Acetic Acid → HCID 178472507, compound

https://huagongshe.com/reaction/2404100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethanolHCID 887—
Reactantethyl (3R)-piperidine-3-carboxylateHCID 185582—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant6-(trans-4-Tert-butylcyclohexyloxy)-2-naphthaldehydeHCID 86668412—
ProductHCID 178472507HCID 178472507—

Reaction Steps

6-(4-tert-Butyl-cyclohexyloxy)-naphthalene-2-carbaldehyde (500 mg, 2 mmol) was combined with (R)-piperidine-3-carboxylic acid ethyl ester (0.51 g, 3.2 mmol) in methanol (10 mL, 200 mmol) and acetic acid (9.2 μL, 0.16 mmol). Sodium cyanoborohydride (0.25 g, 4.0 mmol) was then added and the reaction was stirred overnight at room temperature. The reaction was then quenched with water and extracted three times with ethyl acetate. Organics were combined and dried over MgSO4. Solids were removed via filtration and 10 g of silica gel was added. All solvent was then removed and the resulting silica gel was loaded onto a 24 g column and the product was eluted using a gradient of 0-60% ethyl acetate/hexanes and then dried under vacuum to give the title compound as a colorless oil. EDI-MS: 438.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802659B2
Source datasetuspto-grants-2014_08
ORD IDord-ea18c0de14bf4fa4be0d39e662b62f86
Source noteuspto-grants-2014_08