Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Taurine | HCID 1123 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Nitrobenzyl chloroformate | HCID 78205 | — |
| Solvent | Diethylether water | HCID 21584184 | — |
| Product | HCID 22458570 | HCID 22458570 | 70.7% |
Reaction Steps
A mixture of 2-aminoethanesulfonic acid (5.0 g) and sodium carbonate (9.4 g) in ethyl ether-water (100 mL, 1:1, v/v), at 0° C., was treated with 4-nitrobenzyl chloroformate (8.6 g). After stirring vigorously at 0° C. for 10 min and at room temperature for 15 hr, ethyl ether was added to the reaction mixture. The precipitates were collected by filtration and washed with ethyl ether to afford the title compound (9.2 g) as a white powder: 1H NMR (400 MHz, D2O) δ 2.94 (t, J=6.4 Hz, 2H), 3.39 (t, J=6.4 Hz, 2H), 5.09 (s, 2H), 7.44 (d, J=8.3 Hz, 2H), and 8.11 (d, J=8.3 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06399629B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-440df451cf9b4ef9b23cfc295d1f21bf |
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| Source note | uspto-grants-2002_06 |
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