HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-Chloro-m-nitrotoluene → Methyl(3-nitrobenzyl)sulfane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-Chloro-m-nitrotoluene | HCID 12078 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl(3-nitrobenzyl)sulfane | HCID 22031873 | 100.4% |
Reaction Steps
Sodium methanethiolate (13.5 g; 192 mmol) was added in two portions to a stirred solution of 1-(chloromethyl)-3-nitrobenzene (30.0 g; 175 mmol) in ethanol (360 mL) at −15° C. The cold bath was removed and the batch was stirred at room temperature for 3 hours. The batch was diluted with brine and extracted with ethyl acetate (2×). The combined organic phases were washed with water, dried (sodium sulfate), filtered and concentrated to give the desired product (32.2 g) that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09108926B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-29cce6b31e0e4c788e331f24e4255fd9 |
| Source note | uspto-grants-2015_08 |