HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Propanone, 1-(acetyloxy)-3-chloro- → 3-acetoxy-2-oxopropyl N-(2,3,4-trifluorophenyl)dithiocarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Propanone, 1-(acetyloxy)-3-chloro- | HCID 38413 | — |
| Reactant | N,N-diethyl-1-ethanaminium N-(2,3,4-trifluorophenyl)carbamodithioate | HCID 16413959 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-acetoxy-2-oxopropyl N-(2,3,4-trifluorophenyl)dithiocarbamate | HCID 20030313 | 64% |
Reaction Steps
Triethylammonium N-(2,3,4-trifluorophenyl)dithiocarbamate (2.15 g) prepared in the same manner as in Reference Example 1 was added to methylene chloride (30 ml) and thereto 1-acetoxy-3-chloroacetone (1.0 g) was added dropwise at 2° to 7° C. with stirring over a period of 10 minutes. The mixture was stirred for 20 minutes and washed with 3N hydrochloric acid and then with water. The organic layer was dried over anhydrous magnesium sulfate and then the solvent was distilled off under reduced pressure. The residue was recrystallized from a mixed solvent of hexane ethyl acetate to give the title compound (1.43 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808584 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-76108f6188324cd18932f5b35ba3790a |
| Source note | uspto-grants-1989_02 |