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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669623Generated: November 4, 2026

Tetrahydrofuran → HCID 13140128, compound

https://huagongshe.com/reaction/1669623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantL-LeucinolHCID 111307—
ProductHCID 13140128HCID 13140128—

Reaction Steps

(S)-2-amino-4-methylpentan-1-ol (0.276 ml, 2.133 mmol) was added to a stirred, ice-bath cooled suspension of KH (267 mg, 2.327 mmol) in THF (10 ml) under nitrogen. The resulting mixture was allowed to warm to room temperature and stirred for ˜10 minutes and then treated with Mel (0.121 ml, 1.939 mmol). After stirring for 30 minutes the reaction mixture was quenched by addition of saturated NH4Cl(aq) (˜20 ml) and extracted with EtOAc (25 ml×2). The combined organic phases were dried over MgSO4, filtered under vacuum and the filtrate was evaporated to afford an orange oil. The oil was purified by chromatography on silica eluting with 10% (2M NH3 in MeOH)/DCM to afford the title compound which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989497B2
Source datasetuspto-grants-2011_08
ORD IDord-a3598690d98945afa733252f5fd26268
Source noteuspto-grants-2011_08