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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078994Generated: November 2, 2026

1,7-Heptanediol → 7-Trimethylsiloxy-1-heptanol

https://huagongshe.com/reaction/1078994

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,7-HeptanediolHCID 12381—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventTetrahydrofuranHCID 8028—
Product7-Trimethylsiloxy-1-heptanolHCID 18970908—

Reaction Steps

A solution of 1,7-heptandiol (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 7-trimethylsiloxy-1-heptanol . To a solution of 7-trimethylsiloxy-1-heptanol (11.6 mmol) in dry dichloromethane (50 mL) is added 2,6-di-tert-butyl-4-methylpyridine (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 7-trimethylsiloxy-1-heptyl triflate (50) which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550251
Source datasetuspto-grants-1996_08
ORD IDord-81a4198324bd4d8dbdef6d1527d89cd4
Source noteuspto-grants-1996_08