Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Chlorothiophenol | HCID 7815 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 10927507 | HCID 10927507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18432371 | HCID 18432371 | — |
Reaction Steps
0.8 g (2 mmol) of 1-chloro-2-(8-chloro-4,4-dimethyl-1,1-dioxothiochroman-7-yl)carbonylcyclohex-1-en-3-one was dissolved in 10 ml of tetrahydrofuran and 0.29 g (2 mmol) of 4-chlorothiophenol and 0.22 g (2.2 mmol) of triethylamine were added dropwise. The mixture was stirred at 25° C. for 2 hours, stirred into water, extracted with ethyl acetate and the organic phases were extracted with 1N hydrochloric acid and dried, and the solvent was removed. This gave 0.9 g of beige crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06440899B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-7b1c1aca87574be9b739f000055c69b9 |
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| Source note | uspto-grants-2002_08 |
|---|