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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174018Generated: November 1, 2026

Tetrahydrofuran → HCID 23079270, compound

https://huagongshe.com/reaction/1174018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23079212HCID 23079212—
SolventMethanolHCID 887—
ProductHCID 23079270HCID 2307927075.6%

Reaction Steps

The compound (2.03 g) obtained in Example 127-4 was dissolved in methanol (60.9 ml) and THF (30.5 ml) and, under ice-cooling, added with sodium borohydride (0.442 g), followed by stirring at room temperature for 2 hours. The reaction solution was added with a saturated aqueous ammonium chloride solution and then subjected to separation/extraction with chloroform. The organic layer was dried with anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified through silica gel column chromatography (hexane/ethyl acetate), thereby obtaining the subject compound (1.54 g) as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833991B2
Source datasetuspto-grants-2010_11
ORD IDord-9c301779befd4cd9a46897e9fd3d8827
Source noteuspto-grants-2010_11