Chloro-N,N-dimethylformiminium chloride → 2-Formyl-4,5,7,8-tetrahydro-thieno[2,3-d]azepine-6-carboxylic acid ethyl ester

HRID 627062Notes

Reaction equation

HRID 627062 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

6

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

  1. temperatureto cool to RT
  2. extractionThe resulting solution was extracted with DCM (3×)
  3. washThe combined DCM extracts were washed with water, brine
  4. dry with materialdried over MgSO4
  5. filtrationThe resulting mixture was filtered
  6. 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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