HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399731Generated: October 26, 2026
Ammonium Hydroxide → HCID 18944941, compound
https://huagongshe.com/reaction/399731
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2,6-Dimethylpiperazine | HCID 66056 | — |
| Reactant | O-(o-Aminophenoxy)benzoic acid lactam | HCID 72374 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18944941 | HCID 18944941 | 60.4% |
Reaction Steps
To a stirred solution of 10,11-dihydro-dibenz[b,f][1,4]oxazepin-11-one (0.4 g; 1.9 mmol; Aldrich) in dry toluene (20 mL) at room temperature was added 2,6-dimethyl piperazine (0.99 g; 8.7 mmol; Aldrich) followed by the dropwise addition of TiCl4 (1M in toluene, 2.27 mL; 2.27 mmol). The reaction mixture was refluxed for 2 hours, cooled to room temperature and then poured into an ammonium hydroxide solution (30%, 50 mL). The resulting mixture was extracted with dichloromethane (4×75 mL), and the combined organic phases were then dried (K2CO3) and concentrated. Purification of the product was conducted on silica gel using CHCl3 :MeOH (94:6) eluant to give 0.353 g (60%) of 11-(3,5-dimethyl-1-piperazinyl)-dibenz[b,f][1,4]oxazepine as a pale yellow solid; m.p. 112°-114° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05824676 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-775a3fd0caea4ceba23b815c6b802f9f |
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| Source note | uspto-grants-1998_10 |
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