Reaktionsgleichung
[S:1]1[C:5]([C:6](O)=[O:7])=[CH:4][C:3]2[CH2:9][CH2:10][CH2:11][CH2:12][C:2]1=2.C(Cl)(=O)C([Cl:16])=O>ClCCl.CN(C)C=O>[S:1]1[C:5]([C:6]([Cl:16])=[O:7])=[CH:4][C:3]2[CH2:9][CH2:10][CH2:11][CH2:12][C:2]1=2Komponenten
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
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).
Aufarbeitung
- temperatureto warm to RT over 1 hour
- customAll solvent is then removed under reduced pressure
- customto remove residual oxalyl chloride
- dissolutionThe residue is then dissolved in ethyl acetate
- washwashed with saturated sodium bicarbonate (1×100 mL)
- washwashed with saturated sodium chloride (1×100 mL)
- dry with materialdried over sodium sulfate
- filtrationThe solution is then filtered
- concentrationconcentrated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-87845a04017d4e2bbbc86c4637470a31
- Quelldatensatz
- uspto-grants-2011_02
- Patentnummer
- US07884108B2
Verknüpfte Notizen
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