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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198229Generated: November 1, 2026

Hydrochloric Acid → Acetoxy-1-(3-chlorophenyl)-2-(2-tertbutoxyethoxy)ethane

https://huagongshe.com/reaction/1198229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant1-(3-Chlorophenyl)-2-(2-tertbutoxyethoxy)ethanolHCID 53835502—
SolventDichloromethaneHCID 6344—
ProductAcetoxy-1-(3-chlorophenyl)-2-(2-tertbutoxyethoxy)ethaneHCID 53824717—

Reaction Steps

37.0 g of 1-(3-chlorophenyl)-2-(2-tertbutoxyethoxy)ethanol was dissolved in 70 ml of methylene chloride. To the solution were added 12.9 q of pyridine and 16.6 g of acetic anhydride. The resulting mixture was stirred for 24 hours at room temperature. The reaction mixture was added to a mixture of 150 ml of ice water and 100 ml of methylene chloride. The resulting mixture was adjusted to pH 2 with 6N hydrochloric acid. The organic layer was separated, washed with a saturatred aqueous sodium hydrogencarbonate solution and water in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure to obtain 40.0 g of oily 1 acetoxy-1-(3-chlorophenyl)-2-(2-tertbutoxyethoxy)ethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05280032
Source datasetuspto-grants-1994_01
ORD IDord-b7e6ce97baef4968b43e1af3e15ce49c
Source noteuspto-grants-1994_01