Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | HCID 44550855 | HCID 44550855 | — |
| Product | HCID 44549153 | HCID 44549153 | 39% |
Reaction Steps
Solid 174 (57 mg, 0.16 mmol) was dissolved in cone. H2SO4 (5 mL) at 0° C., then treated dropwise with a cold (0° C.) solution of KNO3 (16 mg, 0.16 mmol) in cone. H2SO4 (0.5 mL). After 15 min, the mixture was poured into ice water and extracted with CH2Cl2 (×6). The combined organic extracts were washed with water (×2), brine and dried. Chromatography eluting with petroleum ether/EtOAc (7:3) gave 8-acetyl-1-(chloromethyl)-5-nitro-3-(trifluoroacetyl)-1,2-dihydro-3H-benzo[e]indole (175) (25 mg, 39%) as an orange powder: mp (petroleum ether/EtOAc) 196-198° C.; 1H NMR (CDCl3) δ 9.23 (s, 1H), 8.58 (d, J=9.1 Hz, 1H, 8.49 (d, J=1.3 Hz, 1H), 8.17 (dd, J=9.1, 1.6 Hz, 1H), 4.73 (d, J=11.5 Hz, 1H), 4.56 (dd, J=11.4, 8.8 Hz, 1H), 4.47-4.39 (m, 1H), 3.98 (dd, J=11.6, 3.6 Hz, 1H), 3.77 (dd, J=11.6, 7.8 Hz, 1H), 2.78 (s, 3H). Anal. (C17H12ClF3N2O4) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07718688B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-c62d26edf066469f8ec6af6acc3a5c5d |
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| Source note | uspto-grants-2010_05 |
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