HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl orthoformate → Tert-butyl 3,3-dimethoxycyclopentanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | tert-Butyl 3-oxocyclopentane-1-carboxylate | HCID 14009986 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | Tert-butyl 3,3-dimethoxycyclopentanecarboxylate | HCID 58784445 | 90.1% |
Reaction Steps
To a solution of tert-butyl 3-oxocyclopentanecarboxylate (19.8 g, 107 mmol) in 1:1 DCM/methanol (150 mL) was added trimethylorthoformate (46.8 mL, 428 mmol), followed by TsOH.H2O (˜0.5 g). The reaction mixture was stirred at room temperature for 2 h. Then more TsOH.H2O (˜0.25 g) was added and the reaction mixture was stirred overnight. The reaction mixture was concentrated at room temperature and the resulting residue was dissolved in ether and washed with saturated NaHCO3 solution, then with brine. The ethereal layer was dried over anhydrous MgSO4, filtered, and concentrated. Purification by flash chromatography (silica, 15% ethyl acetate/hexane) gave 22.2 g (90%) of tert-butyl 3,3-dimethoxycyclopentanecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07598243B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-54082dc2ff724e2185a44c42f5c845fa |
| Source note | uspto-grants-2009_10 |