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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390382Generated: October 26, 2026

Acetic Acid → HCID 18335092, compound

https://huagongshe.com/reaction/390382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantBenzyl 1,2-dihydrospiro[indole-3,4'-piperidine]-1'-carboxylateHCID 10914256—
SolventMethanolHCID 887—
ProductHCID 18335092HCID 1833509275.1%

Reaction Steps

To a 0° C. solution of benzyl spiro[indoline-3,4′-piperidine]-1′-carboxylate (1.15 g, 3.56 mmol), formaldehyde (37% aqueous solution, 1.44 mL, 17.83 mmol) and acetic acid (1.02 mL, 17.83 mmol) in methanol (25 mL) is added sodium cyanoborohydride (0.67 g, 10.68 mmol). The reaction mixture is allowed to warm to room temperature overnight. The pH of the mixture is adjusted to approximately 8 with 10% NaHCO3 solution and extracted with EtOAc (3×50 mL). The combined extracts are washed with water (50 mL) and brine (50 mL), dried, filtered, and evaporated to dryness. The crude material is purified by silica gel chromatography, eluting with hexane:ethyl acetate (85:15) to give the title compound as an off-white solid (0.9 g, 75%). ESI/MS m/z 337.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383642B2
Source datasetuspto-grants-2013_02
ORD IDord-987ca30390754174bccf5de80f935aa9
Source noteuspto-grants-2013_02