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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963968Generated: October 31, 2026

Methyl 4-cyanooxane-4-carboxylate → [4-(Aminomethyl)oxan-4-yl]methanol

https://huagongshe.com/reaction/1963968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-cyanooxane-4-carboxylateHCID 16726727—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product[4-(Aminomethyl)oxan-4-yl]methanolHCID 22379474—

Reaction Steps

To the crude product from step 1 (0.944 g, 5.58 mmol) in THF (5 ml) (a dark brown solution) at 0° C. was added LAH (5.58 ml, 5.58 mmol) dropwise via a syringe. The brown mixture was warmed to room temperature and stirred for 18 hours. The resulting mixture was yellow cloudy. LC/MS showed containing desired product. To the reaction was added sodium sulfate decahydrate solid at 0° C. The mixture was stirred at room temperature for 20 min., then filtered and washed with DCM. The yellow filtrate was concentrated in vacuo to give 0.74 g of orange oil. This crude material was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415381B2
Source datasetuspto-grants-2013_04
ORD IDord-45fcb659298a49e0b6687d8a8cc883d6
Source noteuspto-grants-2013_04