HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172925Generated: November 2, 2026
Benzyl 4-Hydroxybenzoate → HCID 59556611, compound
https://huagongshe.com/reaction/1172925
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl 4-Hydroxybenzoate | HCID 7180 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 59556611 | HCID 59556611 | 98% |
Reaction Steps
In a 100 mL round bottomed flask benzyl 4-hydroxybenzoate (1.445 g, 6.33 mmol) and potassium carbonate (4.17 g, 30.1 mmol) in acetone (100 ml) were combined. Tert-butyl 2-bromoacetate (0.908 ml, 6.03 mmol) was added dropwise. The solution was stirred at 65° C. overnight. The solution was cooled then, the reaction mixture was filtered through a sintered glass funnel. The filtrate was concentrated to afford pale yellow oil, which was purified via silica gel chromatography (40 g, 30% EtOAc:Heptane) to afford benzyl 4-(2-tert-butoxy-2-oxoethoxy)benzoate (2.06 g, 5.90 mmol, 98% yield) as colorless oil. LC/MS (Table 1, Method a) Rt=4.31 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834039B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-19f1f934b8ae425da13920920e379db8 |
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| Source note | uspto-grants-2010_11 |
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