HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726850Generated: October 26, 2026
Hydrochloric Acid → 3-Difluoromethoxy-2-(o-tolyl)acrylic acid methyl ester
https://huagongshe.com/reaction/726850
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 15-Crown-5 | HCID 36336 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Methyl 2-(2-methyl phenyl)-3-hydroxy-2-propenoate | HCID 67027340 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 3-Difluoromethoxy-2-(o-tolyl)acrylic acid methyl ester | HCID 53849144 | — |
Reaction Steps
Preparation of ##STR8## 7.76 g of the sodium salt of 3-hydroxy-2-(o-tolyl)-acrylic acid methyl ester and 0.3 g of 15-crown-5 in 160 ml of N-methyl-2-pyrrolidone (NMP) are cooled to 5° C. with stirring. Chlorodifluoromethane is then passed in while simultaneously adding dropwise a solution of 8.5 g of sodium hydroxide in 9.3 ml of water and the reaction mixture is left to react with vigorous stirring at 5°-8° C. for 2 hours. 82 ml of 2N hydrochloric acid are then added dropwise at 0°-8° C. and the phases are separated. The aqueous phase is extracted exhaustively with ethyl acetate and the combined organic phases are washed with a saturated sodium chloride solution. After drying over sodium sulfate, the residue is filtered and concentrated to dryness by evaporation in vacuo. 3-difluoromethoxy-2-(o-tolyl)acrylic acid methyl ester is obtained in the form of a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05710314 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-99071d58d85a48c1917e9a38df6e2781 |
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| Source note | uspto-grants-1998_01 |
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