Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Fluoroethanol | HCID 9737 | — |
| Reactant | HCID 20189638 | HCID 20189638 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13363520 | HCID 13363520 | 80.9% |
Reaction Steps
To a solution of 6-amino-8-ethoxy-1,3-benzodioxane (1.95 g) in toluene (20 ml), a toluene solution containing phosgene (10 g) was dropwise added at 10° to 20° C. The resultant mixture was heated gradually and, after being refluxed for 30 minutes, cooled to room temperature. The solvent was removed in vacuo, whereby crude 8-ethoxy-1,3-benzodioxan-6-ylisocyanate was obtained. This crude substance was dropwise added to a toluene solution (50 ml) containing triethylamine (1.0 g) and 2-fluoroethanol (0.70 g) at room temperature. The resultant mixture was allowed to stand at room temperature for 12 hours, poured into ice-water and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography using a mixture of toluene and ethyl acetate as the eluent to give 2-fluoroethyl N-(8-ethoxy-1,3-benzodioxan-6-yl)carbamate (Compound No. 10) (2.31 g) in a yield of 80.9%. M.P., 154° -154.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04686232 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-5eb2f821488b423cbb3ed018620cc075 |
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| Source note | uspto-grants-1987_08 |
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