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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479167Generated: October 31, 2026

Ethanol → HCID 72722442, compound

https://huagongshe.com/reaction/1479167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantHCID 90078497HCID 90078497—
SolventTetrahydrofuranHCID 8028—
ProductHCID 72722442HCID 7272244288%

Reaction Steps

The methyl 4-[2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-sulphonyl)-ethyl]benzoate (3.54, 8.54 mmol) is placed in solution in 256 ml of tetrahydrofuran, 25.6 ml of ethanol and 12.8 ml of water in a round-bottomed flask. 3.54 g of lithia monohydrate are added. The whole mixture is stirred for 4 hours at reflux. Ambient the reaction medium is concentrated by half, taken up with ethyl acetate and water and then brought to pH6 with 2N HCl. After extraction, the organic phase is washed with a saturated NaCl solution, dried over MgSO4, concentrated and washed with ether. 3 g of 4-[2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-sulphonyl)ethyl]benzoic acid are obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09408793B2
Source datasetuspto-grants-2016_08
ORD IDord-a22572ae5e894ac195c3d547c0547440
Source noteuspto-grants-2016_08