HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → (-)-3-t-Butyldimethylsilyloxybutyric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-(tert-Butyldimethylsiloxy)butyric acid methyl ester | HCID 13712779 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (-)-3-t-Butyldimethylsilyloxybutyric acid | HCID 13712781 | 95% |
Reaction Steps
To a solution of 3.58 g (15.4 mmol) of methyl (-)-3-t-butyldimethylsilyloxybutyrate dissolved in 30 ml of methanol, 30 ml of 1N potassium hydroxide was added and the mixture was stirred for 15 hours. After almost all methanol was distilled away, the resultant was acidified with 1N hydrochloric acid and extracted with diethyl ether. The extract was washed with a saturated solution of NaCl, dried with anhydrous magnesium sulfate and concentrated under reduced pressure to give 3.18 g of (-)-3-t-butyldimethylsilyloxybutyric acid (yield: 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05081238 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-bcb5c6e0d3654d4cb57ce5f4e68ec316 |
| Source note | uspto-grants-1992_01 |