HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397475Generated: October 27, 2026
Sulfuric Acid → 2-Bromomethylphenylacetic acid t-butyl ester
https://huagongshe.com/reaction/397475
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | [2-(Bromomethyl)phenyl]acetic acid | HCID 12889260 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Bromomethylphenylacetic acid t-butyl ester | HCID 59085879 | — |
Reaction Steps
To a solution of 80 g (0.349 mol) 2-bromomethylphenylacetic acid in 700 mL 1,4-dioxane in a 2 L heavy-walled flask was added 84 mL (1.571 mol) concentrated sulfuric acid at ambient temperature. The reaction mixture was chilled to −15° C., and 580 mL isobutylene was condensed directly into the reaction vessel. The sealed pressure flask was shaken mechanically at room temperature for 4 h (the pressure inside the flask rises to ca. 20 psi during this step). The mixture was carefully quenched by slowly pouring it into a 0-5° C. stirred mixture of 1.2 L tert-butyl methyl ether and 336 g (4.0 mol) solid sodium bicarbonate before slow dilution with 1.2 L ice-water. The separated organic phase was washed with 0.8 L brine, dried with sodium sulfate, filtered concentrated in vacuo to give an oil, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610701B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-7e5bab0db56749dea4088df587c46272 |
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| Source note | uspto-grants-2003_08 |
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