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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368830Generated: October 31, 2026

Tetrahydrofuran → 2-(Isochroman-1-yl)-2-methylpropionic acid

https://huagongshe.com/reaction/368830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-(isochroman-1-yl)-2-methylpropionateHCID 23288833—
SolventEthanolHCID 702—
Product2-(Isochroman-1-yl)-2-methylpropionic acidHCID 23288894—

Reaction Steps

Sodium hydroxide (1N, 12 ml) is added dropwise over several minutes, followed by a few mls of THF (to aid in solution) to a mixture of methyl 2-(isochroman-1-yl)-2-methylpropionate (LXXI, 1.833 g, 7.8 mmol) in ethanol (12 ml). The mixture is stirred overnight at 20-25°, then at 47° for 2 hr, followed by stirring at 20-25° over the weekend. Additional THF and sodium hydroxide (1N, 12 ml) are added and the mixture is stirred overnight at 20-25° and then at 40° for 7 hr, followed by overnight at 20-25°. Ethanol is then removed under reduced pressure and the resulting solids are dissolved in water. The aqueous phase is separated and washed twice with hexane to remove any unreacted starting material and the aqueous phase is then cooled in an ice/water bath and hydrochloric acid (4N, 6 ml) is added dropwise. The mixture is extracted three times with ether and the combined organic phases are backwashed with saline, dried over magnesium sulfate, and concentrated. Recrystallization from dichloromethanemexane gives 2-(isochroman-1-yl)-2-methylpropionic acid (LXXII), mp 110.5-115.75°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133446
Source datasetuspto-grants-2000_10
ORD IDord-6def33753c594eb9a3217cf485d70631
Source noteuspto-grants-2000_10