HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 4-chloro-3-nitrobenzoate → Methyl 4-(methylsulfanyl)-3-nitrobenzenecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 4-chloro-3-nitrobenzoate | HCID 735797 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 4-(methylsulfanyl)-3-nitrobenzenecarboxylate | HCID 21187831 | 62.7% |
Reaction Steps
A solution of methyl 4-chloro-3-nitrobenzoate (28 g) in acetone (250 mL) is treated portionwise with sodium thiomethoxide (10 g) and the mixture is stirred overnight at room temperature. After filtration, the solution is concentrated and water (300 mL) is added to the residue. The yellow solid is filtered off and subjected to flash chromatography eluting with a mixture of diethyl ether and pentane (1:4 v/v), to give methyl 4-methylthio-3-nitrobenzoate (18.5 g), in the form of a yellow solid, m.p. 118°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05840724 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-4374b5e7f1844a5da42b094d9d49608d |
| Source note | uspto-grants-1998_11 |