Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 68702921 | HCID 68702921 | — |
| Solvent | Dioxane Methanol | HCID 21966525 | — |
| Product | HCID 68700711 | HCID 68700711 | 72% |
Reaction Steps
A solution of 6 (1.00 g, 2.05 mmol) in a dioxane/MeOH (1:1, 20 mL) was treated at 10° C. with 4N aqueous KOH (5 mL), and stirred at 10° C. for 45 min. The mixture was acidified to pH 2 with1 N aqueous HBr, concentrated to a small volume under reduced pressure, and then diluted with saturated aqueous NaBr (20 mL). The resulting semi-solid was isolated and crystallized twice from MeOH/H2O to give 5-[bis(2-bromoethyl)amino]-4-(methylsulfonyl)-2-nitrobenzoic acid (7) (0.70 g, 72%): mp 174-176° C.; 1H NMR [(CD3)2SO] δ 8.50 (s, 1 H), 7.88 (s, 1 H), 3.79 (t, J=7.0 Hz, 4 H), 3.62 (t, J=7.0 Hz, 4 H), 3.48 (s, 3 H). Anal. (C12H14Br2N2O6S) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07629332B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-25671ca5cdb545089aee45864ecfd684 |
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| Source note | uspto-grants-2009_12 |
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