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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217957Generated: November 3, 2026

Trimethyl orthoformate → Tert-butyl 3,3-dimethoxycyclopentanecarboxylate

https://huagongshe.com/reaction/2217957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
Reactanttert-Butyl 3-oxocyclopentane-1-carboxylateHCID 14009986—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventDichloromethane methanolHCID 21226129—
ProductTert-butyl 3,3-dimethoxycyclopentanecarboxylateHCID 5878444590.1%

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. 1H NMR (500 MHz, CDCl3): 3.21 (s, 3H), 3.20 (s, 3H), 2.80 (m, 1H), 2.10 to 1.80 (bm, 6H), 1.46 (s, 9H). 13C NMR (125 MHz, CDCl3): 174.9, 111.2, 80.3, 67.8, 49.2, 42.5, 37.4, 33.8, 28.3, 22.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410961B2
Source datasetuspto-grants-2008_08
ORD IDord-d5bde6c48314465dbadfcdabbeacc353
Source noteuspto-grants-2008_08