Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198228Generated: November 2, 2026

2-(Tert-butoxy)ethan-1-ol → 1-(3-Chlorophenyl)-2-(2-tertbutoxyethoxy)ethanol

https://huagongshe.com/reaction/1198228

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tert-butoxy)ethan-1-olHCID 24232—
Reactant2-(3-Chlorophenyl)oxiraneHCID 155613—
ReactantPotassium tert-butoxideHCID 23665647—
SolventEthyl AcetateHCID 8857—
Product1-(3-Chlorophenyl)-2-(2-tertbutoxyethoxy)ethanolHCID 53835502—

Reaction Conditions

Temperature80 °C

Reaction Steps

5.1 g of potassium tert-butoxide was added to 105 ml of ethylene glycol mono-tert-butyl ether. The mixture was heated to 80° C. Thereto was dropwise added 35.0 g of 2-(3-chlorophenyl)oxirane over 1 hour. The mixture was stirred for 2 hours at the same temperature. The reaction mixture was added to a mixture of 100 ml of ice water and 100 ml of ethyl acetate. The organic layer was separated, washed with a saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue thus obtained was subjected to further distillation under reduced pressure to obtain 37.7 g of colorless oily 1-(3-chlorophenyl)-2-(2-tert-butoxyethoxy)ethanol having a boiling point of 140°-146° C./0.9 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05280032
Source datasetuspto-grants-1994_01
ORD IDord-6404ec34562249b5a16439671422a572
Source noteuspto-grants-1994_01