Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 2-Fluoro-N-(2-fluoro-2,2-dinitroethyl)-2,2-dinitro-ethylamine | HCID 140338 | — |
| Reactant | Ethyl 3-chlorothiophene-2-carboxylate | HCID 12993676 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Product | HCID 13015160 | HCID 13015160 | — |
Reaction Steps
A mixture of 55.0 g (0.19 mol) of bis(2-fluoro-2,2-dinitroethyl)amine, 38 ml of chloroform, 40 ml of ethyl chlorothiolformate and 20 ml of titanium tetrachloride was heated in an oil bath at 65°-67° C. for 17 hours (The reaction mixture was protected from atmospheric moisture with a drierite drying tube). Chloroform (100 ml) was added to the warm mixture which was then filtered through celite. The dark colored filtrate was pulled on a rotary evaporator to give a residue which was dissolved in methanol and treated with charcoal. After filtration, the solvent was removed with a rotary evaporator and the product was crystallized by dissolving in chloroform (55 ml) and cooling in the freezer. The yield was 48.0 g (67%), mp 74°-75° C., NMR (chloroform): δ1.26(t), 2.95(q), 4.83(d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04311649 |
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| Source dataset | uspto-grants-1982_01 |
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| ORD ID | ord-f08df5c39d8c4745816ac1fdd182e6d2 |
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| Source note | uspto-grants-1982_01 |
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