Chloro-N,N-dimethylformiminium chloride → 2-Formyl-4,5,7,8-tetrahydro-thieno[2,3-d]azepine-6-carboxylic acid ethyl ester
Reaction equation
[CH2:1]([O:3][C:4]([N:6]1[CH2:12][CH2:11][C:10]2[CH:13]=[CH:14][S:15][C:9]=2[CH2:8][CH2:7]1)=[O:5])[CH3:2].C[N+](C)=CCl.[Cl-].[C:22]([O-])(=[O:24])C.[Na+]>ClCCCl.O>[CH2:1]([O:3][C:4]([N:6]1[CH2:12][CH2:11][C:10]2[CH:13]=[C:14]([CH:22]=[O:24])[S:15][C:9]=2[CH2:8][CH2:7]1)=[O:5])[CH3:2]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 70 °C
Procedure
To a stirred solution of 4,5,7,8-tetrahydro-thieno[2,3-d]azepine-6-carboxylic acid ethyl ester (1.50 g, 6.65 mmol) in 1,2-dichloroethane (20 ml) was added Vilsmeier reagent (1.49 g, 11.65 mmol). The reaction mixture was heated to 70° C. for 5 hours. The reaction mixture was allowed to cool to RT followed by addition of 1 M sodium acetate (20 ml). The mixture was vigorously stirred for 2 hours and then diluted with water (50 ml). The resulting solution was extracted with DCM (3×). The combined DCM extracts were washed with water, brine, and dried over MgSO4. The resulting mixture was filtered and solvent evaporated in vacuo to give the subtitled compound as a tan oil (1.56 g) that was used without further purification. MS: ESI (positive): 254 (M+H).
Workup
- temperatureto cool to RT
- extractionThe resulting solution was extracted with DCM (3×)
- washThe combined DCM extracts were washed with water, brine
- dry with materialdried over MgSO4
- filtrationThe resulting mixture was filtered
- customsolvent evaporated in vacuo
Sources & evidence
- ORD record
- ord-09001223f1834233a908aeb7db706795
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09309262B2
Reaction notes
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