HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709192Generated: October 29, 2026
3-Chlorothiophene → 2-Acetyl-3-chlorothiophene
https://huagongshe.com/reaction/709192
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chlorothiophene | HCID 87017 | — |
| Reactant | N-Methoxy-N-methylacetamide | HCID 537505 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-Acetyl-3-chlorothiophene | HCID 1487253 | 104.6% |
Reaction Steps
To a solution of 3-chlorothiophene (4.80 g, 40.48 mmol) in THF (50 mL) was added BuLi (2.5N in hexane, 17.9 mL) at −30° C. After addition, the mixture was stirred for 30 min at −10° C., and then cooled to −45° C. N-methoxy-N-methyl acetamide (55.0 g, 48.8 mmol) was added and allowed to warm to room temperature during 40 min and maintained for an additional 20 min. Brine (80 mL) was added to quench the reaction, extracted with EA (60 mL×3). The combined organic layers were dried over anhydrous Na2SO4, filtered, concentrated to afford 24-1 (˜80% pure) as a yellow oil (6.80 g) which used for the next step directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09180119B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-205a27d2b5b54695bb0d25281f1778d2 |
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| Source note | uspto-grants-2015_11 |
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