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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | 2-(4-Bromophenyl)ethanol | HCID 72851 | — |
| Catalyst | Ammonium Chloride | HCID 25517 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(4-(2-hydroxyethyl)phenyl)-2-methylpropanoate | HCID 45257528 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08487106B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-2d4650c2785e4eb4aaa3015244304ef6 |
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| Source note | uspto-grants-2013_07 |
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