Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Isopropyl 5-amino-2-chlorobenzoate | HCID 369590 | — |
| Reactant | 3-Methyl-5,6-dihydro-1,4-dioxine-2-carboxylic acid | HCID 15376174 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21470253 | HCID 21470253 | — |
Reaction Steps
A mixture of thionyl chloride (1.3 g, 0.011 mole) and 5,6-dihydro-3-methyl-1,4-dioxin-2-carboxylic acid (0.57 g, 0.004 mole) was refluxed on a steam bath for 3 hours and the excess thionyl chloride was evaporated at atmospheric pressure. The resulting liquid was added dropwise to a stirred solution of 1-methylethyl 5-amino-2-chlorobenzoate (1.6 g, 0.008 mole) in diethyl ether (30 ml), cooled in an ice-water bath. The mixture was worked up by diluting with diethyl ether (120 ml), washing with dilute hydrochloric acid (50 ml), and then with water (50 ml). The diethyl ether solution was dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure, leaving a solid residue. The crude product was washed with isopropyl alcohol (30 ml), leaving a brown solid, m.p. 103°-105° C. (1.2 g, 95.8% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05693827 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-d39eb9cfd6d047c0a4358153541269c8 |
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| Source note | uspto-grants-1997_12 |
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