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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451226Generated: October 29, 2026

Hydrochloric Acid → Methyl 2-(4-(2-hydroxyethyl)phenyl)-2-methylpropanoate

https://huagongshe.com/reaction/451226

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetonitrileHCID 6342—
ReactantEthyl AcetateHCID 8857—
ReactantHexamethyldisilazaneHCID 13838—
Reactant2-(4-Bromophenyl)ethanolHCID 72851—
CatalystAmmonium ChlorideHCID 25517—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(4-(2-hydroxyethyl)phenyl)-2-methylpropanoateHCID 4525752888%

Reaction Steps

In a reaction vessel, 4-bromo phenethyl alcohol (5.0 g), hexamethyldisilizane (HMDS; 3.0 g), acetonitrile (25 mL) and ammoniumchloride (0.01 g) were introduced, and the mixture was stirred at room temperature for 1 hours or more. The mixture was condensed under reduced pressure, and dichloromethane (30 mL) and distilled water (20 mL) were added to separate layers. The separated organic layer was dehydrated with Na2SO4, and then, condensed by filtration. And then, Pd(dba)2 (0.29 g), t-Bu3P (0.20 g), ZnF2 (1.28 g), methyltrimethylsilyl dimethylketene acetal (2.2 g) and DMF (50 mL) were added thereto, and the mixture was reacted at 80□ for 18 hours. Distilled water (75 mL), ethylacetate (75 mL) and 1N hydrochloric acid (9 mL) were added thereto, and the mixture was stirred to separate layers. The separated organic layer was dehydrated with Na2SO4, and then condensed by filtration, and purified to obtain 2-[4-(2-hydroxy-ethyl)-phenyl]-2-methyl-propionic acid methylester (5.2 g, yield 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487106B2
Source datasetuspto-grants-2013_07
ORD IDord-2d4650c2785e4eb4aaa3015244304ef6
Source noteuspto-grants-2013_07