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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078993Generated: October 31, 2026

1,5-Pentanediol → HCID 18970864, compound

https://huagongshe.com/reaction/1078993

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 numberUS05550251
Source datasetuspto-grants-1996_08
ORD IDord-d81d409644ca41d7b06452e5ad62e231
Source noteuspto-grants-1996_08