HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 19961482, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 2,2-Dichloro-1,1,1,3,3-pentafluoropropane | HCID 62315 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Product | HCID 19961482 | HCID 19961482 | — |
Reaction Steps
Until HCFC-225a becomes available in commercial quantities, HCFC-225a may be prepared by a standard and well-known organic synthesis technique. For example, 2,2-dichloro-1,1,1,3,3-pentafluoropropane may be prepared by reacting a dimethylformamide solution of 1,1,1-trichloro-2,2,2-trifluoromethane with chlorotrimethylsilane in the presence of zinc, forming 1-(trimethylsiloxy)-2,2-dichloro-3,3,3-trifluoro-N,N-dimethylpropylamine. The 1-(trimethylsiloxy)-2,2-dichloro-3,3,3-trifluoro-N,N-dimethylpropylamine is reacted with sulfuric acid to form 2,2-dichloro-3,3,3-trifluoropropionaldehyde. The 2,2-dichloro-3,3,3-trifluoropropionaldehyde is then reacted with sulfur tetrafluoride to produce 2,2-dichloro-1,1,1,3,3-pentafluoropropane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05288819 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-c46419f82f82418090768d4cb6a6639d |
| Source note | uspto-grants-1994_02 |