Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-Methoxybenzenethiol | HCID 84989 | — |
| Reactant | 2-Chloroethylamine hydrochloride | HCID 9793737 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 24697918 | HCID 24697918 | 95% |
Reaction Steps
A mixture of 3-methoxybenzenethiol (5 g), 2-chloroethylamine hydrochloride (1.1 eq.) and Cs2CO3 (2.2 eq.) in CH3CN (60 mL) was stirred at 60° C. for 20 h. To the reaction mixture, EtOAc (100 mL) was added, and washed with H2O (2×30 mL). The organic phase was concentrated under reduced pressure to give product 20 (Yield: 6.2 g, 95%), which appeared to be pure by TLC and NMR and was used for the next step reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618282B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-047c30e6965b473b808f5416d33296cc |
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| Source note | uspto-grants-2013_12 |
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