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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704897Generated: October 30, 2026

tert-Butanol → HCID 10889004, compound

https://huagongshe.com/reaction/704897

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantAtropic acidHCID 68114—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 10889004HCID 1088900454.8%

Reaction Steps

A stirred suspension of 2-chloro-1-methylpyridinium iodide (3.28 g, 12.8 mmol) in toluene (20 mL) was treated under an atmosphere of nitrogen with atropic acid (1.80 g, 12.2 mol) treated with tert-butanol (0.92 mL, 11.8 mmol), treated with triethylamine (3.6 mL, 25.8 mmol), heated under reflux for 2 hours, cooled to room temperature and treated with water (100 mL) and diethyl ether (100 mL). The layers were separated and the aqueous layer extracted with diethyl ether (50 mL). The organic phases were combined, washed with water (100 mL), dried (MgSO4), evaporated in vacuo, and the residue purified by chromatography [silica; hexane-ethyl acetate (20:1)] to give tert-butyl 2-phenylpropenoate (1.32 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988814
Source datasetuspto-grants-1991_01
ORD IDord-05f034be382d4854981e23d9d8fdf8cb
Source noteuspto-grants-1991_01