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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264044Generated: October 30, 2026

2-(Tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-pyran-4-ol → 2-(tert-Butyl-dimethyl-silanyloxymethyl)-tetrahydro-pyran4-one

https://huagongshe.com/reaction/1264044

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-pyran-4-olHCID 131722841—
SolventDMSO triethylamineHCID 86583882—
Product2-(tert-Butyl-dimethyl-silanyloxymethyl)-tetrahydro-pyran4-oneHCID 13172284066%

Reaction Steps

A solution of 2-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-pyran-4-ol (2.27 g, 9.21 mmol) in anhydrous DMSO/Et3N (15/13 mL) was treated with sulfur trioxide pyridine complex (7.33 g, 46.1 mmol) portionwise at room temperature. After stirring for 1 hour, the reaction was concentrated and the residue was partitioned between EtOAc (100 mL) and water (50 ml). The separated organic layer was washed with brine (70 mL), dried over sodium sulfate, and concentrated. Purification by silica gel column using 10-20% of EtOAc in hexane afforded 1.48 g (66%) of colorless oil: 1H NMR (CDCl3) δ 0.05 (s, 6H), 0.88 (s, 9H), 2.32 (dt, 1H), 2.41 (m, 2H), 2.58 (m, 1H), 3.62 (m, 2H), 3.70 (d, 2H), 4.31 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541481B2
Source datasetuspto-grants-2003_04
ORD IDord-9063fce370f54feba94f41182478313a
Source noteuspto-grants-2003_04