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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377704Generated: October 31, 2026

Acetic Acid → HCID 22914698, compound

https://huagongshe.com/reaction/1377704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-Aminobenzyl alcoholHCID 21439—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-tert-Butyl 3-methyl 4-oxopiperidine-1,3-dicarboxylateHCID 11276893—
SolventMethanolHCID 887—
ProductHCID 22914698HCID 22914698—

Reaction Steps

Methyl 1-Boc-4-oxo-3-piperidinecarboxylate from Step 1 above (3.86 g, 15 mmol) was combined with 2-aminobenzyl alcohol (1.5 g, 12.2 mmol) and acetic acid (1.29 mL, 1.35 g, 22.5 mmol) in methanol (10 mL). Sodium cyanoborohydride (0.94 g, 15 mmol) was added and the mixture was stirred at ambient temperature for 3.5 h. The solvent was removed in vacuo and the residue treated with ethyl acetate (100 mL). The solution was washed with saturated aqueous sodium bicarbonate, dried over sodium sulfate, filtered, and evaporated to dryness in vacuo. The residue was chromatographed on silica gel eluted with 1:4, 1:2, and 3:5 EtOAc:hexane. The combined product fractions were evaporated to dryness in vacuo to give methyl 1-Boc-4-(2-hydroxymethylphenylamino)-3-piperidine carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665719
Source datasetuspto-grants-1997_09
ORD IDord-bfad65b9b7e44f9290ac36d8f8e90fb4
Source noteuspto-grants-1997_09