HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 888427Erstellt: 26. Oktober 2026
Oxalyl chloride → 4,5,6,7-Tetrahydro-benzo[b]thiophene-2-carbonyl chloride
https://huagongshe.com/reaction/888427
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 | DMF dimethylformamide | HCID 17824068 | — |
| 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 dimethylformamide [DMF] under nitrogen and cooled to 0° C. Oxalyl chloride (13.7 mL of a 2.0M solution in ACM) 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 | US08247550B2 |
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| Quelldatensatz | uspto-grants-2012_08 |
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| ORD ID | ord-7e3449f1b0114adf835f25c7c6a279bf |
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| Quellennotiz | uspto-grants-2012_08 |
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