Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium sulfide nonahydrate | HCID 73972 | — |
| Reactant | 1-(Benzyloxy)-2-chloro-3-nitrobenzene | HCID 14356121 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58303835 | HCID 58303835 | — |
Reaction Steps
To a solution of 8.56 g (32.5 mmol) of 1-(benzyloxy)-2-chloro-3-nitrobenzene in 120 mL of DMF was added 15.6 g (64.9 mmol) of pulverized sodium sulfide nonahydrate. The mixture was stirred vigorously at 22° C. for 30 hours and then poured into a vigorously stirred mixture of ether and 1 N HCl. The organic layer was washed with water then brine, dried (Na2SO4), and evaporated. The residue was crystallized from dichloromethane (DCM) and hexane to give 2-(benzyloxy)-6-nitrobenzenethiol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501727B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-1a9ba1d883fc4afa9f25825215dda737 |
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| Source note | uspto-grants-2013_08 |
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