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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323925Generated: October 26, 2026

Diethyl Ether → 2-Trimethylsilyloxy-2-pentene

https://huagongshe.com/reaction/323925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant2-PentanoneHCID 7895—
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilyl triflateHCID 65367—
SolventDichloromethaneHCID 6344—
Product2-Trimethylsilyloxy-2-penteneHCID 5457387149.4%

Reaction Steps

In 500 mL of dichloromethane, was dissolved 22.0 mL (207 mmol) of 2-pentanone. While stirring the resulting solution in an ice bath, 44 mL (317 mmol) of triethylamine was added to the solution, and then, 42 mL (232 mmol) of trimethylsilyl trifluoromethanesulfonate was added dropwise to the solution. After the addition of trimethylsilyl trifluoromethanesulfonate, the mixture was stirred for 1 hour at room temperature, poured into ether (500 mL)/a saturated aqueous sodium hydrogencarbonate solution (300 mL) so as to extract the ether layer. The ether layer was washed with saturated sodium chloride water and water, dried over sodium sulfate anhydride, filtered, and concentrated. The residue was distilled under normal pressure to collect fractions of 110 to 125° C. As a result, 8.43 g (53.2 mmol, 49.4%) of 2-trimethylsilyloxy-2-pentene was obtained. According to a similar method, 5.33 g (33.6 mmol, 32.3%) of 2-trimethylsilyloxy-2-pentene was obtained from 11.0 mL (103.8 mmol) of 2-pentanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06215016B1
Source datasetuspto-grants-2001_04
ORD IDord-c16bb04a563b429eb2cd9a94e017979e
Source noteuspto-grants-2001_04