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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159943Generated: October 31, 2026

4-(Tert-butyldimethylsilyloxymethyl)pyridine → HCID 86618779, compound

https://huagongshe.com/reaction/1159943

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Tert-butyldimethylsilyloxymethyl)pyridineHCID 10987880—
ReactantO-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 11830845—
SolventDichloromethaneHCID 6344—
ProductHCID 86618779HCID 86618779—

Reaction Steps

A solution of 2-[(aminooxy)sulfonyl]-1,3,5-trimethylbenzene (4.05 g, 18.8 mmol) in DCM (60 mL) was cooled to 0° C. 4-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-methyl)pyridine (3.50 g, 15.7 mmol) in DCM (2 mL) was added dropwise. Following complete addition, the mixture was stirred at rt for 45 min. The reaction mixture was evaporated under reduced pressure to give the product as a colorless foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812022B2
Source datasetuspto-grants-2010_10
ORD IDord-d09df32a04744d058aee5f7709a1f9af
Source noteuspto-grants-2010_10