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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280809Generated: October 30, 2026

Water → HCID 15829116, compound

https://huagongshe.com/reaction/2280809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant2,6-Di-tert-butyl-4-methylpyridineHCID 98898—
Reactant1-Methylbicyclo[2.2.1]heptan-2-oneHCID 143613—
SolventDichloromethaneHCID 6344—
ProductHCID 15829116HCID 1582911614%

Reaction Steps

To a solution of methylbicyclo[2.2.1]heptan-2-one (26 g, 0.209 mol) and 2,6-di-tert-butyl-4-methyl-pyridine (64 g, 0.315 mol) in DCM (300 mL) was added dropwise trifluoromethanesulfonic anhydride (88 g, 0.315 mol) in DCM (50 mL) at 0° C. The reaction mixture was stirred at room temperature for 24 h. The mixture was poured into water, and extracted with DCM (2×100 mL). The combined extracts were washed with a 10% hydrochloric acid solution (3×100 mL), saturated aqueous sodium bicarbonate solution (50 mL), brine (50 mL) and dried over sodium sulfate. Concentration under reduced pressure gave the crude product, which was purified by silica gel column chromatography (100% n-pentane) to give the desired product (7.6 g, 0.03 mol, 14%). 1H NMR (400 MHz, CDCl3): δ ppm 5.15 (brs, 1H), 4.89 (brs, 1H), 2.51-2.39 (m, 2H), 2.26-2.17 (m, 2H), 2.12-2.05 (m, 2H), 1.99-1.85 (m, 2H), 1.53-1.50 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139534B2
Source datasetuspto-grants-2015_09
ORD IDord-0481d6cf1dd5473ea0fda159de86e37f
Source noteuspto-grants-2015_09