HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238396Generated: October 30, 2026
Ammonia → 1-(chloromethyl)-7-cyano-5-nitro-1,2-dihydro-3H-benzo[e]indole
https://huagongshe.com/reaction/2238396
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | tert-butyl 1-(chloromethyl)-7-cyano-1,2-dihydro-3H-benzo[e]indole-3-carboxylate | HCID 44550490 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 1-(chloromethyl)-7-cyano-5-nitro-1,2-dihydro-3H-benzo[e]indole | HCID 44549401 | 62.6% |
Reaction Steps
Powdered carbamate 143 (1.00 g, 2.9 mmol) was added portionwise to stirred conc. H2SO4 (10 mL) at 0° C., and the mixture was warmed to room temperature for 10 min. The resulting solution was cooled to −5° C. and treated dropwise with a solution of KNO3 (324 mg, 3.2 mmol) in cone. H2SO4 (2 mL). After siting for a flirter 5 min at 0° C., the mixture was poured into ice/water and neutralized with dilute aqueous NH3. The resulting solid was purified by chromatography on silica gel, eluting with CH2Cl2, followed by recrystallization from CH2Cl2, then EtOAc, to give 1-(chloromethyl)-7-cyano-5-nitro-1,2-dihydro-3H-benzo[e]indole (144) (522 mg, 62%) as a red solid: mp 237-238° C.; 1H NMR [(CD3)2SO] δ 8.55 (d, J=1.4 Hz, 1H), 7.98 (d, J=8.8 Hz, 1H), 7.77 (s, 1H), 7.74 (dd, J=8.8, 1.5 Hz, 1H), 6.87 (s, 1H), 4.29-4.21 (m, 1H), 3.94-3.85 (m, 2H), 3.80 (dd, J=11.1, 8.1 Hz, 1H), 3.75 (dd, J=10.6, 3.1 Hz, 1H). Anal. (C14H10ClN3O2) C, H, N, Cl.
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-16733de696af4bf68a33aece65ac4956 |
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| Source note | uspto-grants-2010_05 |
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