Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | HCID 178418336 | HCID 178418336 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22102064 | HCID 22102064 | — |
Reaction Steps
The inside of a 100 ml three-necked round-bottom flask, to which a dropping funnel is connected, was replaced with nitrogen, then a 1.0M diethyl ether solution (22 ml) of benzyl magnesium chloride was added and the mixture was cooled in an ice bath to 0° C. To this, carbon disulfide (1.32 ml) was dropped from a dropping funnel over 10 minutes, then the mixture was stirred at 0° C. for 4.5 hours. Thereafter, 30 ml of water was added, the mixture was returned to room temperature, the mixture was then washed with diethyl ether (total 100 ml) 2 times. Diethyl ether (50 ml) and 30% HCl (5 ml) were added and the product was extracted from the organic layer. Thereafter, the product was washed with water (total 150 ml) 3 times. The diethyl ether layer was concentrated to obtain phenylethyl dithiocarboxylic acid (1.86 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796386B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-93821316a4914398b3a83417c4ba8b6f |
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| Source note | uspto-grants-2014_08 |
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