HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1363487Erstellt: 24. Oktober 2026
Oxalyl chloride → 4,5,6,7-Tetrahydro-benzo[b]thiophene-2-carbonyl chloride
https://huagongshe.com/de/reaction/1363487
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | 4,5,6,7-Tetrahydro-1-benzothiophene-2-carboxylic acid | HCID 2063443 | — |
| Katalysator | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4,5,6,7-Tetrahydro-benzo[b]thiophene-2-carbonyl chloride | HCID 6485362 | — |
Reaktionsschritte
4,5,6,7-Tetrahydro-benzo[b]thiophene-2-carboxylic acid (1.0 g, 5.50 mmol) is dissolved in dichloromethane [DCM] (25 mL) that contains 5 drops of N,N-dimethylformamide [DMF] under nitrogen and cooled to 0° C. Oxalyl chloride (13.7 mL of a 2.0M solution in DCM) is added via syringe and allowed to warm to RT over 1 hour. All solvent is then removed under reduced pressure, and the resultant oil is reduced from toluene (3×20 mL) to remove residual oxalyl chloride. The residue is then dissolved in ethyl acetate and washed with saturated sodium bicarbonate (1×100 mL), then washed with saturated sodium chloride (1×100 mL) and dried over sodium sulfate. The solution is then filtered and concentrated under reduced pressure to give 4,5,6,7-tetrahydro-benzo[b]thiophene-2-carbonyl chloride (8) as an off-white solid (1.03 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07884108B2 |
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| Quelldatensatz | uspto-grants-2011_02 |
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| ORD ID | ord-87845a04017d4e2bbbc86c4637470a31 |
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| Quellennotiz | uspto-grants-2011_02 |
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