HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355849Generated: October 28, 2026
Sodium Hydroxide → HCID 67624997, compound
https://huagongshe.com/reaction/355849
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 54524882 | HCID 54524882 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67624997 | HCID 67624997 | 90.8% |
Reaction Steps
A mixture of 0.975 g of 6,11-dihydro-5H-dibenz[b,e]azepine and 0.20 g of NaH (60% in oil) in 20 ml of tetrahydrofuran is stirred at room temperature for 0.5 hr. Then 1.1 g of mono-methyl terephthalyl chloride (prepared from mono-methyl terephthalate and thionyl chloride) is added and the mixture refluxed 18 hours. The mixture is cooled, poured into ice water and filtered. The solid is triturated with dichloromethane-hexane to give 1.0 g of crystals, m.p. 182°-185° C. The preceding compound, methyl 4-[(6,11-dihydro-5H-dibenz[b,e]azepin-5-yl)carbonyl]benzoate (2.11 g), 20 ml of 2N NaOH and 20 ml of methanol is stirred overnight and then heated on a steam bath for 1 hr. The solvent is removed to give a solid. The solid is extracted with ether (discarded). The solid is dissolved in water and the solution acidified with citric acid to give a solid. The solid is filtered and washed with water to give 1.84 g of crystals, m.p. 220°-225° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834461 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-ae8c2022058a431789b93eb1afd7abd4 |
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| Source note | uspto-grants-1998_11 |
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