HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18060Generated: October 30, 2026
Tetrahydrofuran → HCID 68586097, compound
https://huagongshe.com/reaction/18060
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-(Methanesulfonylmethyl)benzoic acid | HCID 4962583 | — |
| Reactant | HCID 17908456 | HCID 17908456 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68586097 | HCID 68586097 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741316B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-1b6b0f04f21e4f3b97941b6a3249547d |
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| Source note | uspto-grants-2010_06 |
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