Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | HCID 15392095 | HCID 15392095 | — |
| Reactant | 4-Methylbenzene-1-sulfonic acid--5,6,7,7a-tetrahydrothieno[3,2-c]pyridin-2(4H)-one (1/1) | HCID 45108320 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | p-Toluenesulfonic acid | HCID 6101 | — |
Reaction Steps
A mixture of 5.00 g of 5,6,7,7a-tetrahydro-4H-thieno[3,2 -c]pyridin-2-one-p-toluenesulfonate, 2.47 g of tert-butyl-dimethylchlorosilane, 1.66 g of triethylamine and 15 ml of methylene chloride was stirred at room temperature (20° C.) for 3 hours. The produced 2-(tert-butyldimethylsilyloxy)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine.p-toluenesulfonate was not isolated, 2.40 g of 2-chlorobenzyl chloride and 3.02 g of triethylamine were added thereto, and the mixture was allowed to react under stirring at 40° C. for 8 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05874581 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-7dad5dac702e483eb0de331a78fc79f7 |
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| Source note | uspto-grants-1999_02 |
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