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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594824Generated: November 1, 2026

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

https://huagongshe.com/reaction/1594824

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 numberUS06284764B1
Source datasetuspto-grants-2001_09
ORD IDord-b626d4b580404e96bd49b7757ed1c3e8
Source noteuspto-grants-2001_09