HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646134Generated: October 29, 2026
Sulfuryl chloride → ethyl 5-bromo-3-chloro-1H-indole-2-carboxylate
https://huagongshe.com/reaction/646134
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Ethyl 5-Bromoindole-2-carboxylate | HCID 259091 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | ethyl 5-bromo-3-chloro-1H-indole-2-carboxylate | HCID 28330549 | 85.8% |
Reaction Steps
A mixture of 5-bromoindole-2-carboxylic acid ethyl ester (4.00 g, 14.9 mmol), sulfurylchloride (1.8 mL, 22.4 mmol) and benzene (125 mL) was stirred at 90° C. for 2.5 h. The mixture was cooled to room temperature, NaHCO3 (aq., sat.) was added and the mixture extracted with EtOAc. The combined extracts were washed with water, brine and dried over Na2SO4. Concentration and recrystallisation (from toluene) gave the sub-title compound (3.87 g 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07705023B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-c74f13d42db74672aa0be2dd38094c51 |
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| Source note | uspto-grants-2010_04 |
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