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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399324Generated: October 30, 2026

1,5-Pentanediol → HCID 18970864, compound

https://huagongshe.com/reaction/399324

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-PentanediolHCID 8105—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18970864HCID 18970864—

Reaction Steps

A solution of 1,5-pentandiol (44 mmol) in THF (15 mL) is cooled to 0° C. and treated with sodium hydride (44 mmol) followed by tert-butyldimethylsilyl chloride (44 mmol). The reaction mixture is stirred at room temperature overnight. Concentration in vacuo and flash chromatography affords 5-trimethylsiloxy-1-pentanol. To a solution of 5-trimethylsiloxy-1-pentanol (11.6 mmol) in dry dichloromethane (50 mL) is added 2,6-di-tert-butyl-4methylpyridine (4.6 g, 22.2 mmol) and triflic anhydride (3.7 mL, 22.2 mmol) at 0° C. The reaction is stirred at room temperature for 20 min, poured into water, and extracted with dichloromethane. The combined extracts are dried over anhydrous sodium sulfate and concentrated in vacuo and to afford 5-trimethylsiloxy-1-pentyl triflate (45) which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05817879
Source datasetuspto-grants-1998_10
ORD IDord-74b7192603964530afc066f65a969a50
Source noteuspto-grants-1998_10