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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278843Generated: November 4, 2026

Acetate → HCID 22252776, compound

https://huagongshe.com/reaction/1278843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 22252725HCID 22252725—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 22252776HCID 22252776—

Reaction Steps

The acetate obtained above is saponified and the resulting hydroxyl group is then protected according to the following procedure: tert-Butyldimethylsilyl chloride (2.64 g) is added to a mixture of 5-(3-bromo-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yloxy)pentan-1-ol (4.3 g, 11.7 mmol) and 80% sodium hydride (422 mg) in THF (20 ml). The mixture is stirred at room temperature for 2 h. The solution is poured into a mixture of water and ethyl acetate. The organic phase is washed twice with water, dried over magnesium sulphate and concentrated on a rotary evaporator under vacuum at 40° C. The product is purified by flash chromatography on a column of silica.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06444709B1
Source datasetuspto-grants-2002_09
ORD IDord-398532e4782146b4ac7e6a96488efac9
Source noteuspto-grants-2002_09