HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016076Generated: October 30, 2026
Ethyl Acetate → Ethyl 2-(fluoromethyl)prop-2-enoate
https://huagongshe.com/reaction/1016076
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Acrylic acid, 2-(hydroxymethyl)-, ethyl ester | HCID 24827 | — |
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-(fluoromethyl)prop-2-enoate | HCID 12815505 | 56% |
Reaction Steps
To a solution of ethyl 2-(hydroxymethyl)acrylate (5 g, 38 mmol) in 50 mL of methylene chloride was added DAST (6.0 mL, 46.1 mmol) at −78° C. The reaction mixture was stirred at −78° C. for 1 h, then warmed up to room temperature and continuously stirred overnight. 20 mL of saturated NaHCO3 aqueous solution and 20 mL of ethyl acetate were added to quench the reaction. The organic layer was separated, and the aqueous layer was extracted twice with EtOAc (20 ml×2). The combined organic extracts were dried over MgSO4 and evaporated to give an oil residue (2.8 g, yield: 56%). MS (m/z): 131 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985730B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-7695bf841da041079ccc1c444a71973a |
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| Source note | uspto-grants-2011_07 |
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