HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704682Generated: October 29, 2026
Hydrochloric Acid → HCID 14349082, compound
https://huagongshe.com/reaction/704682
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 14349062 | HCID 14349062 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14349082 | HCID 14349082 | 45% |
Reaction Steps
A solution of 7,8-dimethoxy-1-phenoxy-2,3,4,5-tetrahydro-3-benzazepine of Example 35 (6.5 g, 22 mmole) in 300 ml methanol was acidified to pH 1 with ethereal hydrogen chloride. After this solution was cooled with an ice bath, N-bromosuccinimide (4.2 g, 24 mmole) was added. The reaction mixture slowly warmed to ambient temperature, was evaporated, stirred with water, basified with saturated sodium carbonate and was extracted with ethyl acetate-ether. The organic extracts were washed with water, saturated sodium chloride and were dried (anhydrous MgSO4), filtered and evaporated to 8 g of any oil. This oil was converted to the maleate salt (8 g, 74%, m.p. 95°-100° C.) by the addition of ethereal maleic acid of which 4 g was recrystallized twice from isopropanol-ether to give 2.4 g (45%) of 1-(4-bromophenoxy)-7,8-dimethoxy-2,3,4,5-tetrahydro-3-benzazepine maleate, d 145°-146° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04988690 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-51f52b23d3694df4a3d9e42d14ad6ec9 |
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| Source note | uspto-grants-1991_01 |
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