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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080735Generated: November 1, 2026

Tetrahydrofuran → HCID 23079270, compound

https://huagongshe.com/reaction/2080735

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 11-4 was dissolved in methanol (61 ml) and THF (31 ml) and added with sodium borohydride (0.442 g) under ice-cooling and the whole was stirred at room temperature for 2 hours. The reaction solution was added with a saturated aqueous ammonium chloride solution and then subjected to 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 numberUS07932281B2
Source datasetuspto-grants-2011_04
ORD IDord-4359a12870554bf49d4e39c6f5c3160a
Source noteuspto-grants-2011_04