HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901103Generated: October 26, 2026
1-Bromo-3-chloropropane → 5-(3-Chloro-propoxy)-1H-indole-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/901103
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 5-hydroxy-1H-indole-2-carboxylate | HCID 90677 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 5-(3-Chloro-propoxy)-1H-indole-2-carboxylic acid ethyl ester | HCID 45112356 | 74% |
Reaction Steps
To a solution of ethyl-5-hydroxyindole-2-carboxylate (15 g, 73 mmol, 1.0 eq.) and 1-bromo-3-chloropropane (8.8 mL, 88 mmol, 1.2 eq.) in 2-butanone (200 mL) was added potassium carbonate (12.1 g, 88 mmol, 1.2 eq.). The reaction mixture was stirred 160 h at 80° C. The reaction mixture was cooled down and partitioned between ethyl acetate and water. The aqueous phase was extracted with ethyl acetate. The combined organic phases were washed with water and brine then dried over sodium sulfate, filtered and concentrated in vacuo. The crude mixture was purified by column chromatography on silica eluting with cyclohexane/ethyl acetate 9:1 to yield 15.3 mg (74%) of the title compound as a light yellow solid. MS (m/e): 282.7 (MH+, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07361682B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-891340eab47746c18ea2a6b9e9b1bd4d |
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| Source note | uspto-grants-2008_04 |
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