HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025252Generated: November 1, 2026
Benzyl Alcohol → Benzyl 2-bromo-2,2-difluoroacetate
https://huagongshe.com/reaction/1025252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Benzyl 2-bromo-2,2-difluoroacetate | HCID 10378165 | 58% |
Reaction Steps
1.60 g (14 mmol) of t-butoxypotassium was added to a solution prepared by dissolving 20.30 g (0.1 mol) of ethyl 2-bromo-2,2-difluoroacetate in 140 ml of benzyl alcohol and 1200 ml of hexane at 0° C. in a nitrogen atmosphere. The mixture was stirred at 0° C. for 1 hour. After confirming disappearance of the raw materials by thin-layer chromatography (TLC), the reaction was terminated by adding 120 ml of concentrated hydrochloric acid. The mixture was washed twice with water, washed twice with a saturated sodium chloride solution, and dried over anhydrous sodium sulfate. After evaporating the solvent under reduced pressure, the product was purified by column chromatography to obtain 15.37 g of benzyl 2-bromo-2,2-difluoroacetate shown by the following formula (yield: 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08728706B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-9264c0c0b74e4c7eb3037507ccd5ffd2 |
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| Source note | uspto-grants-2014_05 |
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