HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 6-{[tert-Butyl(dimethyl)silyl]oxy}hexanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 123778939 | HCID 123778939 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Product | 6-{[tert-Butyl(dimethyl)silyl]oxy}hexanoic acid | HCID 12717311 | 90% |
Reaction Steps
A solution of 3.25 g (9.02 mmol) of the bissilylated compound 6-[(tert-butyldimethyl-silyl)oxy]-hexanoic acid silyl ester in 130 ml of methanol and 44 ml of ThF is mixed with a solution of 4.4 g (31.8 mmol, 3.5 equivalents) of K2CO3 in 44 ml of H2O, and it is stirred for 1 hour at room temperature. Then, the volume of reaction solution is reduced to one-fourth in a vacuum. It is diluted with 130 ml of saturated NaCl solution and set at pH 4-5 with 1 M KHSO4 solution. It is extracted with diethyl ether. The combined organic phases are dried on MgSO4, and the solvent is distilled off in a rotary evaporator. 2.01 g (8.17 mmol) of 6-[(tert-butyldimethylsilyl)oxy]-hexanoic acid, corresponding to a yield of 90%, is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06156905 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-f910670726ed48c9bb039ecf291d0c18 |
| Source note | uspto-grants-2000_12 |