Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | HCID 14127516 | HCID 14127516 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 14127517 | HCID 14127517 | — |
Reaction Steps
To a solution of 40.7 ml of thiophosgene in 300 ml of dry diethyl ether at -78° C. was added dropwise a solution of 20 g of diphenyl-(2-methylprop-2-yl)silyl 4-hydroxybenzoate and 8.5 ml of triethylamine. After having been stirred for a further 30 minutes at -78° C. and 90 minutes at room temperature, the mixture was partitioned between diethyl ether and water. The organic layer was washed with water and brine, was dried over calcium chloride, and then evaporated in vacuo to afford 25.9 g of an orange oil. Crromatography over silica gel and elution with hexane-ethyl acetate mixtures afforded 16.8 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04795748 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-e9d440a675074c38ad735e1f3ed491c8 |
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| Source note | uspto-grants-1989_01 |
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