HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894340Generated: October 26, 2026
2-Bromopropane → Ethyl alpha-fluoro-alpha-isopropyl-4-chlorophenylacetate
https://huagongshe.com/reaction/894340
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl alpha-fluoro-4-chlorophenylacetate | HCID 13194587 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl alpha-fluoro-alpha-isopropyl-4-chlorophenylacetate | HCID 13194588 | 62% |
Reaction Steps
A mixture of ethyl α-fluoro-4-chlorophenylacetate (2.3 g), isopropyl bromide (1.10 g), sodium hydride (0.56 g of a 50% mixture in oil), dry hexamethylphosphoramide (6 ml) and dry benzene (6 ml) was heated with stirring at a temperature of 35° C. under nitrogen for a period of 22 hours. The reaction mixture was poured into ice-water and the aqueous mixture extracted with methylene chloride. The methylene chloride extract was dried over anhydrous sodium sulfate and solvent removed by distillation under reduced pressure. The product was chromatographed over silica gel using 15% ethylene dichloride in petroleum ether as eluant to give ethyl α-fluoro-α-isopropyl-4-chlorophenylacetate (1.42 g; 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04283414 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-e15221b6f4434772a0c95961674edcf7 |
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| Source note | uspto-grants-1981_08 |
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