HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365072Generated: October 30, 2026
Ethylenediamine → 5-phenyl-2,3-dihydro-1H-1,4-benzodiazepine
https://huagongshe.com/reaction/1365072
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | 2-Fluorobenzophenone | HCID 67650 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-phenyl-2,3-dihydro-1H-1,4-benzodiazepine | HCID 12336926 | — |
Reaction Steps
A 5 mL microwave tube was charged with 2-fluorobenzophenone (0.40 g), ethylene diamine (0.40 g) and ethanol (4 mL). The mixture was heated in a microwave at 180° C. for 10 minutes. The contents were concentrated to an oil and dissolved in methylene chloride. The resulting solution was purified by silica gel chromatography. Any unreacted benzophenone was eluted with methylene chloride and then the desired product was eluted with 70% ethyl acetate in hexanes. Desired fractions were concentrated to provide 5-phenyl-2,3-dihydro-1H-1,4-benzodiazepine as a yellow crystalline solid. H1 NMR (d6-dmso): 7.30-7.42 (m, 5H), 7.12 (dd, 1H), 6.78 (d, 1H), 6.75 (d, 1H), 6.49 (dd, 1H), 6.05 (br t, 1H), 3.84 (m, 2H), 3.56 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07888503B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-268ea34eb6744ee3b39aa8504e50460c |
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| Source note | uspto-grants-2011_02 |
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