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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241338Generated: October 31, 2026

Pyridine → 160701-58-6

https://huagongshe.com/reaction/1241338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant3-Hydroxyphenethyl alcoholHCID 83404—
SolventDichloromethaneHCID 6344—
Product160701-58-6HCID 1080083581.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-hydroxyphenethyl alcohol (6.0 g, 43.4 mmol) in 275 mL of CH2Cl2 was added 6.55 g (43.4 mmol) of TBDMS-Cl (tert-butyldimethylsilyl chloride), cooled to 0° C., then added 7.0 mL (86.8 mmol) of pyridine. The reaction mixture was stirred at ambient temperature overnight. Upon concentration, the crude mixture was purified by silica gel flash chromatography (eluted with hexane then 5% EtOAc/hexane) to provide 8.9 g of a clear oil: 1H NMR (300 MHz, DMSO-d6) δ 9.17 (s, 1H), 7.04 (m, 1H), 6.60 (m, 3H), 3.73 (t, J=6.9 Hz, 2H), 2,65 (t, J=6.9 Hz, 2H), 0.83 (s, 9H), −0.03 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115589B2
Source datasetuspto-grants-2006_10
ORD IDord-275df6e1484c4b8abed541f2e9d79fa0
Source noteuspto-grants-2006_10