HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076069Generated: October 25, 2026
Methylamine → N-methyl-10,11-dihydro5H-dibenzo[a,d]cyclohepten-5-imine
https://huagongshe.com/reaction/1076069
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Dibenzosuberone | HCID 14589 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-methyl-10,11-dihydro5H-dibenzo[a,d]cyclohepten-5-imine | HCID 21541752 | 90% |
Reaction Steps
A solution of 52.5 g of titanium tetrachloride in 300 ml of anhydrous benzene is added slowly, under nitrogen, to a stirred, cooled (ice-bath) mixture of 100 g of 10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one, 103 g of methylamine and 1200 ml of anhydrous benzene. After stirring at room temperature for 12 days the mixture is cooled, treated with concentrated aqueous sodium bicarbonate solution and filtered through Celite. The layers of the filtrate are separated, and the benzene layer is dried with magnesium sulfate. Removal of the solvent and crystallization of the residue from 200 ml of hexane gives 95.6 g (88% yield) of N-methyl-10,11-dihydro5H-dibenzo[a,d]cyclohepten-5-imine, mp 89°-90°. An analytical sample (hexane) also had mp 89°-90°. Nmr spectrum (in CDCl3): multiplets at τ 2.3-3.2 (8H) and 6.8-7.2 (4H) and singlet at 6.7 (3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03954865 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-8ff2a7a658544ba3ba66873a786c9fb5 |
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| Source note | uspto-grants-1976_05 |
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