HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328581Generated: October 26, 2026
Water → 5-(4-isopropyl-2-morpholinylmethyl)-10,11-dihydro-5H-dibenz[b,f]azepine
https://huagongshe.com/reaction/328581
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Iminodibenyl | HCID 10308 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | 2-(Chloromethyl)-4-(propan-2-yl)morpholine | HCID 12832480 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 5-(4-isopropyl-2-morpholinylmethyl)-10,11-dihydro-5H-dibenz[b,f]azepine | HCID 21442791 | — |
Reaction Steps
To a suspension of sodium amide (0.5 g) in benzene was added a solution of 10,11-dihydro-5H-dibenz[b,f]azepine (1.0 g) in benzene at room temperature, and the resulting mixture was stirred under reflux for 1 hour. After cooling, a solution of 4-isopropyl-2-chloromethylmorpholine (1.0 g) in benzene was added to the reaction mixture at room temperature, and the resulting mixture was stirred at room temperature for 1 hour and refluxed for 20 hours with stirring. The reaction mixture was cooled and admixed with water. The benzene layer was separated, washed with water, dried over anhydrous magnesium sulfate and evaporated to afford 5-(4-isopropyl-2-morpholinylmethyl)-10,11-dihydro-5H-dibenz[b,f]azepine as an oily substance. M.P. 203.5° -- 204.5° C (oxalate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04017621 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-8cadcf62a44d4ee4ba6e649edb8b39cf |
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| Source note | uspto-grants-1977_04 |
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