Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 18696611 | HCID 18696611 | — |
| Product | HCID 18696597 | HCID 18696597 | — |
Reaction Steps
A solution of triphosgene (16.7 g) in ethyl acetate (130 mL) was heated to reflux and a suspension of the title compound of Step D (4.9 g) in ethyl acetate was added via cannula and the aid of a mechanical pump over a period of 40 min. The temperature was held at approximately 75° C. during the addition. After the addition was complete, the reaction mixture was heated at reflux for 2 h, cooled to room temperature and stirred overnight at room temperature. The reaction mixture was poured into a solution of saturated aqueous sodium bicarbonate, extracted with ethyl acetate, and the combined organic extracts were dried (MgSO4), filtered and concentrated under reduced pressure to afford 4.9 g of the title compound of Step E as a white solid melting at 142-143° C. 1H NMR (CDCl3): δ 7.93 (dd,1H), 7.84 (d,1H), 7.43 (m,2H), 7.24 (dd,1H), 6.75 (d,1H), 3.87 (s,3H), 3.62 (s,3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06096895 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-40232a28b4b440a293bfbc706d73444e |
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| Source note | uspto-grants-2000_08 |
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