HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Propanethiol → 1-Nitro-3-[(propan-2-ylsulfanyl)methyl]benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Propanethiol | HCID 6364 | — |
| Reactant | alpha-Chloro-m-nitrotoluene | HCID 12078 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Nitro-3-[(propan-2-ylsulfanyl)methyl]benzene | HCID 70976437 | — |
Reaction Conditions
| Temperature | -15 °C |
|---|
Reaction Steps
A solution of sodium methoxyde (15.5 mL, 25 wt % in methanol) was diluted with methanol (85 mL) and treated with 2-propanethiol (6.3 mL) at room temperature for 60 minutes, cooled to −15° C., treated with 3-nitrobenzylchloride (10 g) in 3 portions, kept for 2 hours at −15° C., then the temperature was increased to room temperature. The reaction mixture was concentrated in vacuo, treated with diethyl ether (300 mL), washed with water (2×100 mL) and brine (100 mL), dried with sodium sulfate and evaporated to dryness. The title compound (12.3 g) was thus obtained and used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08916557B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-83ff9f2f25b74a57b4cd7db9c70d60b8 |
| Source note | uspto-grants-2014_12 |