Réaction #833506

ord-7c6df8408c7d480c9739168e0d4f87a8

Équation de réaction

CN(C)C/C=C/C(=O)O.Cl
4-dimethylaminocrotonic acid hydrochloride
O=C(Cl)C(=O)Cl
oxalyl chloride
CN(C)C/C=C/C(=O)Cl.Cl
4-dimethylaminocrotonoyl chloride hydrochloride
Rendement 72.4%

Solvants

Conditions de réaction

Température
22.5°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurethen cooled to 0° C.
  2. 2
    workup.WAITheld for 30 min
  3. 3
    AutreThe solids were collected on Buchner funnel (under a blanket of nitrogen) and
  4. 4
    Lavagewashed with cold (0° C.) THF (3×5 mL)
  5. 5
    AutreThe product was dried under vacuum (˜1 torr) at 40-50 2° C. for 3 h

Mode opératoire

A well stirred suspension 4-dimethylaminocrotonic acid hydrochloride (5.0 g, 30 mmol) in cold (0° C.) THF (40 mL) and DMF (2 pipet drops) was treated with oxalyl chloride (3.15 mL, 36 mmol). The mixture was stirred at 20-25° C. for 3 h then cooled to 0° C. and held for 30 min. The solids were collected on Buchner funnel (under a blanket of nitrogen) and washed with cold (0° C.) THF (3×5 mL). The product was dried under vacuum (˜1 torr) at 40-50 2° C. for 3 h to give 4.0 g of 4-dimethylaminocrotonoyl chloride hydrochloride. This material is characterized as its methyl ester by treatment of the solid with methanol.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE040418E1uspto-grants-2008_07