HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487209Generated: October 26, 2026
Allyl bromide → Methyl 2,3-dihydro-6-fluoro-4-(2-propenyl)-4H-1-benzopyran-4-carboxylate
https://huagongshe.com/reaction/487209
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl 6-fluorochromane-4-carboxylate | HCID 14986536 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2,3-dihydro-6-fluoro-4-(2-propenyl)-4H-1-benzopyran-4-carboxylate | HCID 19094435 | — |
Reaction Steps
A solution of methyl 6-fluorochromane-4-carboxylate (2.1 g) in anhydrous N,N-dimethylformamide was added to a suspension of sodium hydride (265 mg) in anhydrous N,N-dimethylformamide under nitrogen. After gas evolution ceased, the mixture was cooled to 0° C., and neat allyl bromide (0.95 mL) was added. After 1 hour, 20 mL of an aqueous saturated ammonium chloride solution was added, and the mixture extracted with ethyl acetate, the extracts washed with water, brine, dried over anhydrous sodium sulfate, filtered and evaporated to afford the title compound as a colorless oil, 2.4 g. (HRMS calc'd 250.1004; found 250.1002).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05294635 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-207f89b7fa854ea698902b91f0fa7f70 |
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| Source note | uspto-grants-1994_03 |
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