HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394562Generated: October 29, 2026
Water → Ethyl 5-chloro-3-methyl-1-benzothiophene-2-carboxylate
https://huagongshe.com/reaction/394562
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 19404-18-3 | HCID 317317 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Ethyl 5-chloro-3-methyl-1-benzothiophene-2-carboxylate | HCID 14836260 | 67% |
Reaction Steps
n-Butyllithium in hexane (2.6 M, 2.3 ml) was added to a solution of 5-chloro-3-methylbenzo(b)thiophene (1,0 g, 6 mmol) in ethyl ether-(20 ml) stirred at 0° C. under argon. The mixture was stirred for 30 minutes and transferred slowly under argon pressure to a stirred solution of ethyl chloroformate (0.63 g, 6 mmol) in ethyl ether (20 ml). The mixture was stirred at 0° C. for 30 minutes and at 25° C. for 1.5 hours. The mixture was treated with water and the organic phase was dried, concentrated and triturated with hexane to give 1.0 g (67%) of ethyl 5-chloro-3-methylbenzo(b)thiophene-2-carboxylate: mp 92.5-94° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06602888B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-f80cfe1e10084d64acec56402531a10c |
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| Source note | uspto-grants-2003_08 |
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