HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410656Generated: October 30, 2026
1,2-Dichloroethane → ethyl 6-bromo-8-carbamoyl-2,3,4,9-tetrahydro-1H-carbazole-3-carboxylate
https://huagongshe.com/reaction/2410656
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 6-bromo-3-(ethoxycarbonyl)-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acid | HCID 66604417 | — |
| Solvent | Tetrahydrofurane dichloromethane | HCID 21919333 | — |
| Product | ethyl 6-bromo-8-carbamoyl-2,3,4,9-tetrahydro-1H-carbazole-3-carboxylate | HCID 66605138 | — |
Reaction Steps
To a light suspension of 6-bromo-3-(ethoxycarbonyl)-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acid (2.12 g, 5.79 mmol), EDC (1.332 g, 6.95 mmol), and 1-hydroxybenzotriazole hydrate (1.064 g, 6.95 mmol) in THF/CH2Cl2 (5/1) (100 mL) was added ammonium hydroxide (1.353 mL, 34.7 mmol) and it turned into a thick light yellow suspension and it was stirred at rt overnight. The reaction was concentrated and the residue was dissolved in water/ethyl acetate. The organic phase was separated and washed with brine, dried over Na2SO4, filtered, concentrated to afford the crude product as a light yellow solid, which was washed with a small amount of ether and air-dried. The crude ethyl 6-bromo-8-carbamoyl-2,3,4,9-tetrahydro-1H-carbazole-3-carboxylate was used as such in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815840B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-59692cc74aca41b195eb7a55945689b0 |
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| Source note | uspto-grants-2014_08 |
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