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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772402Generated: October 31, 2026

Tetrahydrofuran → HCID 117817929, compound

https://huagongshe.com/reaction/1772402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 117817964HCID 117817964—
SolventEthanolHCID 702—
ProductHCID 117817929HCID 11781792999.5%

Reaction Steps

Sodium borohydride (1.32 g, 34.83 mmol, 1.5 equiv) was added in portions at 0° C. to a solution of compound 13 (10.0 g, 23.22 mmol, 1.0 equiv), THF (100 mL) and ethanol (100 mL). The reaction mixture was stirred at room temperature overnight, when LCMS indicated that the reaction was complete. The mixture was concentrated under reduced pressure and the residue was diluted with ethyl acetate (300 mL) and water (50 mL). 1M HCl was added dropwise to quench the reaction. The layers were separated and the aqueous layer was extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with saturated brine (500 mL), dried over sodium sulfate, filtered, and concentrated under reduced pressure to give the crude compound 14 (10.0 g, >99% yield) as a pale-yellow oil. This material was used subsequently.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249239B2
Source datasetuspto-grants-2016_02
ORD IDord-251ae77e804041c9b0907a31658ce1ed
Source noteuspto-grants-2016_02