HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 3-Chlorobenzoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-Methyl-1-(4-(methylthio)phenyl)-2-morpholino-1-propanone | HCID 92387 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Chlorobenzoic Acid | HCID 447 | — |
Reaction Steps
A solution of 13 g of m-chloroperbenzoic acid in 50 g of CH2Cl2 is added dropwise, at 0° and while stirring, to a solution of 20 g of 2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one in 200 g of methylene chloride. Stirring is continued for a further 2 hours, in the course of which the m-chlorobenzoic acid formed is deposited in the form of a white precipitate. The reaction mixture is poured into ice/1N NaOH, and the organic phase is separated off, dried over Na2SO4 and evaporated on a rotary evaporator. The crude 2-methyl-1-[4-(methylsulfenyl)phenyl]-2-morpholinopropan-1-one which remains is recrystallised from ethyl acetate/hexane. Melting point 112°-113° C. (Compound No. 31).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04582862 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-0e4bb4809ec44e33b36b76361a0c9829 |
| Source note | uspto-grants-1986_04 |