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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48312Generated: October 27, 2026

Sodium Hydroxide → 5-Mercapto-2,2-dimethylpentanoic acid ethyl ester

https://huagongshe.com/reaction/48312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantThioureaHCID 2723790—
ReactantEthyl 5-bromo-2,2-dimethylpentanoateHCID 10681333—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product5-Mercapto-2,2-dimethylpentanoic acid ethyl esterHCID 1008125274.1%

Reaction Steps

To a solution of 5-bromo-2,2-dimethylpentanoic acid ethyl ester (2.41 g, 10 mmol) in ethyl alcohol (5 mL) was added thiourea (0.77 g, 10 mmol) and the mixture was refluxed for 3 h under a nitrogen atmosphere. A solution of sodium hydroxide (0.62 g, 15 mmol) in deionized water (2.5 mL) was added and stirring was continued for another 2 h at reflux temperature. The mixture was cooled to rt and the ethanol was distilled off under reduced pressure. Diethyl ether (20 mL) was added and the layers were separated. The organic phase was washed with saturated sodium chloride solution (5 mL), dried over sodium sulfate, filtered, and concentrated in vacuo to give 5-mercapto-2,2-dimethylpentanoic acid ethyl ester (1.41 g, 74%) as a yellow oil. 1H NMR (300 MHz, CDCl3/TMS): d (ppm): 4.12 (q, J=7.0 Hz, 2H), 2.57-2.43 (m, 2H), 1.69-1.45 (t, 4H), 1.25 (t, J=7.0 Hz, 3H), 1.17 (s, 7H). 13C NMR(75 MHz, CDCl3/TMS): d (ppm): 177.55, 41.0, 39.24, 25.07, 24.90, 14.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06703422B2
Source datasetuspto-grants-2004_03
ORD IDord-878b5f2ef79b40218137b48bdd1a0bd1
Source noteuspto-grants-2004_03