Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 10927507 | HCID 10927507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18432353 | HCID 18432353 | — |
Reaction Steps
0.7 g (1.75 mmol) of 1-chloro-2-(8-chloro-4,4-dimethyl-1,1-dioxothiochroman-7-yl)carbonylcyclohex-1-en-3-one were dissolved in 10 ml of tetrahydrofuran, and 0.19 g (1.75 mmol) of thiophenol and 0.19 g (1.92 mmol) of triethylamine were added dropwise. The mixture was stirred at 25° C. for two hours and then stirred into water, extracted with ethyl acetate and the organic phases were extracted with 1N hydrochloric acid, dried and concentrated. This gave 0.8 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-8adea02b76b04b1586107a5619d2fd94 |
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| Source note | uspto-grants-2002_08 |
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