HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium hydroxide, monohydrate → Tert-butyl 6-(4-carboxyphenyl)-spiro[2.5]octane-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | MeOH tetrahydrofuran | HCID 21899815 | — |
| Reactant | HCID 66740128 | HCID 66740128 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tert-butyl 6-(4-carboxyphenyl)-spiro[2.5]octane-1-carboxylate | HCID 66739947 | 83.9% |
Reaction Steps
0.159 g of tert-butyl 6-(4-ethoxycarbonylphenyl)spiro[2.5]octane-1-carboxylate (0.44 mmol, 1 eq.) is placed in 4 mL of a 3/1 mixture of THF/methanol in a 50 mL round-bottomed flask. 0.075 g of lithium hydroxide monohydrate (1.78 mmol; 4 eq.) dissolved in 1 mL of water is added with stirring. After 16 hours at room temperature, the reaction medium is evaporated and aqueous 6% sulfur dioxide solution is added. The precipitate is filtered off to give 0.122 g of tert-butyl 6-(4-carboxyphenyl)-spiro[2.5]octane-1-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546391B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-a7235f46bc6b49ce94ea4ba5ff1c3272 |
| Source note | uspto-grants-2013_10 |