Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 74383124 | HCID 74383124 | — |
| Product | HCID 86736123 | HCID 86736123 | — |
Reaction Steps
A 3.3 g (0.028 mol) sample of methylsulfonyl chloride was added slowly to a slurry of 6.5 g (0.027 mol) of the sodium salt of alpha-cyano-2,6-dichlorobenzaldoxime in 60 ml acetone. The reaction was exothermic. After the addition was completed, the reaction mixture was stirred at about 25° C. for 1 hour, filtered and evaporated under reduced pressure to give a tan oil which crystallized to give the product. Recrystallization from ether/hexane gave the product as white crystals, m.p. 81-82. Nuclear magnetic resonance analysis showed the product to be approximately a 60:40 mixture of the syn- and anti-isomers. Elemental analysis for the product is tabulated in Table I as Compound No 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04123255 |
|---|
| Source dataset | uspto-grants-1978_10 |
|---|
| ORD ID | ord-bb9d7052afdf4002baaf53b2b336320c |
|---|
| Source note | uspto-grants-1978_10 |
|---|