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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18060Generated: October 30, 2026

Tetrahydrofuran → HCID 68586097, compound

https://huagongshe.com/reaction/18060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactant3-(Methanesulfonylmethyl)benzoic acidHCID 4962583—
ReactantHCID 17908456HCID 17908456—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 68586097HCID 68586097—

Reaction Conditions

Temperature0 °C

Reaction Steps

(3-Methylsulfonylmethylphenyl)methanol may be prepared by carrying out the procedure in the following manner: a mixture of 26 g of 3-(methylsulfonylmethyl)-benzoic acid and 4.6 g of lithium aluminum hydride in 600 cm3 of tetrahydrofuran is stirred for 18 hours at a temperature close to 20° C. The solution is cooled to 0° C. and then 15 cm3 of ethyl acetate, 30 cm3 of water, 5 cm3 of a 15% aqueous solution of sodium hydroxide and finally 30 cm3 of water are added-successively. The mixture is filtered on celite and the filtrate taken up in 600 cm3 of ethyl acetate. The organic phase is taken up in 500 cm3 of water and then 200 cm3 of a saturated aqueous sodium chloride solution, separated after settling, dried over anhydrous magnesium sulfate, filtered and concentrated to dryness under reduced pressure (2.7 kPa). 10.4 g of (3-methylsulfonyl-methylphenyl)methanol are obtained in the form of a gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741316B2
Source datasetuspto-grants-2010_06
ORD IDord-1b6b0f04f21e4f3b97941b6a3249547d
Source noteuspto-grants-2010_06