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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649544Generated: October 30, 2026

Methanol → 3-Acetoxy-3-(4-chlorophenyl)-3-(3-pyridyl)-1-propene

https://huagongshe.com/reaction/1649544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
Reactant1-(4-Chlorophenyl)-1-(3-pyridyl)-2-propen-1-olHCID 12717098—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetic AnhydrideHCID 7918—
Product3-Acetoxy-3-(4-chlorophenyl)-3-(3-pyridyl)-1-propeneHCID 1271710590%

Reaction Steps

A mixture of 1-(4-chlorophenyl)-1-(3-pyridyl)-2-propen-1-ol (0.692 g, 2.8 mmol), triethylamine (3.3 ml) and 4-dimethylaminopyridine (85 g) was stirred in acetic anhydride (0.9 ml) at 25° C. for 20 h. Methanol (1 ml) was added and after 10 min the mixture was concentrated in vacuo. Ether (25 ml) was added and the ether phase was washed with saturated NaHCO3 solution (3×15 ml) and dried over MgSO4. Evaporation of the solvent gave 0.725 g (90%) of the title compound, which was used in the palladium catalyzed amination according to Example 16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04418065
Source datasetuspto-grants-1983_11
ORD IDord-f3cfc1b4986f496f87277adceebd0a10
Source noteuspto-grants-1983_11