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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595261Generated: October 28, 2026

Sodium borohydride → 7-(Hydroxymethyl)-4-azaspiro[2.4]heptan-5-one

https://huagongshe.com/reaction/595261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-Oxo-4-azaspiro[2.4]heptane-7-carbaldehydeHCID 91618561—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product7-(Hydroxymethyl)-4-azaspiro[2.4]heptan-5-oneHCID 91618414—

Reaction Steps

Sodium borohydride (1.4 g, 6.6 mmol) was added to a stirred solution of 5-oxo-4-azaspiro[2.4]heptane-7-carbaldehyde (0.51 g, 3.3 mmol) in methanol (8 mL) and water (12 mL) at 0° C. The reaction mixture was allowed to warm to room temperature and stirred for 1 hour. The reaction mixture was dried over sodium sulfate and concentrated under reduced pressure to afford the crude product residue. The crude product residue was purified by silica gel chromatography (1:10 methanol in dichloromethane, Rf=0.4) to give 7-(hydroxymethyl)-4-azaspiro[2.4]heptan-5-one. 1H NMR (400 MHz, CD3OD) δ 3.65-3.42 (m, 2H), 2.73-2.55 (m, 1H), 2.46-2.22 (m, 2H), 1.11-0.92 (m, 1H), 0.83-0.59 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242984B2
Source datasetuspto-grants-2016_01
ORD IDord-a153221c65cc478a8b9605a10055c552
Source noteuspto-grants-2016_01