HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450832Generated: October 31, 2026
Water → 2-Chloro-5,6,7,8,9,10-hexahydro-cyclohepta[b]indole-6-carboxylic acid methyl ester
https://huagongshe.com/reaction/450832
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Reactant | Methyl 3-bromo-2-oxocycloheptanecarboxylate | HCID 11507060 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-5,6,7,8,9,10-hexahydro-cyclohepta[b]indole-6-carboxylic acid methyl ester | HCID 11701840 | 53.4% |
Reaction Steps
Methyl 3-bromo-2-oxocycloheptanecarboxylate (16.8 g, 67.4 mmol) and 4-chloroaniline (18.4 g, 98%, 2.13 eq, 143.6 mmol) were added to flask with thermometer, nitrogen inlet and mechanical stirring machine. As the temperature of the mixture passed 140° C. a relatively rapid exotherm and vigorous evolution of gas occurred. The reaction was cooled with water immediately. The reaction mixture was dissolved in DCM (200 mL). The material was transferred into a separatory funnel and washed with water (2×50 mL), 3HCl (3×50 mL), water (2×50 mL), brine, dried over Na2SO4, and the solvent was removed by vacuo. The crude residue was applied to a Biotage and eluted with 9/1 heptane/ethyl acetate to afford product 10 g (53%) as an off white solid, which was used for next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486990B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-9c741fb956784b39a8e6c58c0d9d4e26 |
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| Source note | uspto-grants-2013_07 |
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