HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038024Generated: October 28, 2026
Acrylic acid, 2-(hydroxymethyl)-, ethyl ester → Ethyl 2-(fluoromethyl)prop-2-enoate
https://huagongshe.com/reaction/1038024
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acrylic acid, 2-(hydroxymethyl)-, ethyl ester | HCID 24827 | — |
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-(fluoromethyl)prop-2-enoate | HCID 12815505 | — |
Reaction Steps
To a solution of (diethylamino)sulfur trifluoride (DAST) (363 μl, 2.76 mmol) in dichloromethane (1 ml) was slowly added at −78 C a solution of 2-hydroxylmethyl acrylic acid ethyl ester (300 mg, 2.31 mmol) in dichloromethane (3 ml). The reaction mixture was allowed to warm to room temperature, re-chilled to −78 C and additional DAST (100 μl, 0.76 mmol) was added to ensure complete reaction. The reaction mixture was let to warm to room temperature and quenched with saturated sodium carbonate. Organic layer was isolated, washed with water, brine and dried (MgSO4). The dichloromethane solution was directly passed through a short silica gel pad, eluted with dichloromethane and the product fractions were collected. The combined fractions (ca. 12 ml) will be directly used in the next step synthesis without further concentration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546404B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-df81805611544e569bb2cb8f0cebd729 |
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| Source note | uspto-grants-2013_10 |
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