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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78554Generated: October 24, 2026

Sodium Carbonate → 4-Methyl-4-(methyldisulfanyl)pentanoic acid

https://huagongshe.com/en/reaction/78554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantS-Methyl methanethiosulfonateHCID 18064—
Reactant4-Mercapto-4-methylpentanoic acidHCID 11579156—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-Methyl-4-(methyldisulfanyl)pentanoic acidHCID 1156463470%

Reaction Steps

A solution of mercaptopentanoic acid 7 (6.0 mL, 40 mmol) was dissolved in 50 mL of deionized water in a 250 mL flask. The solution was magnetically stirred as sodium carbonate (6.4 g, 60 mmol) was added to the acid at a rate that would not cause excessive frothing. The flask was equipped with a 100 mL addition funnel, which was charged with a solution of methyl methanethiolsulfonate (7.5 g, 60 mmol) dissolved in 30 mL of glass-distilled 100% ethanol. The flask was cooled in an ice/water bath and the system was maintained under an argon atmosphere. The methyl methanethiolsulfonate solution was added drop-wise to the flask as rapidly as possible but without causing excessive frothing. The cooling bath was removed and the reaction mixture was allowed to stir for an additional 3 hours. Solvent was removed by rotary evaporation under vacuum, until approximately 20 mL remained. After which 10 mL of saturated sodium bicarbonate and 30 mL of deionized water were added. The mixture was washed three times with 25 mL portions of ethyl acetate in a separatory funnel. The aqueous layer was adjusted to approximately pH 2 with 5 M HCl and was extracted twice with 120 mL portions of ethyl acetate. The organic layers were combined and washed with 20 mL of a solution composed of saturated NaCl and 1M HCl at a ratio of 4:1. The organic layer was then dried over 14 g of anhydrous sodium sulfate and solvent was removed by rotary evaporation under vacuum to give 5.4 g of product 8 (70% yield). The material can be taken to the next step without further purification. 1H NMR (CDCl3): δ1.54 (6H, s), 2.15-2.21 (2H, m), 2.64 (3H, s), 2.69-2.72 (2H, m). MS (M+Na+) calc.: 217.0, found: 217.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841425B2
Source datasetuspto-grants-2014_09
ORD IDord-a8b8fd4a1a4d4796877a486b3166cac4
Source noteuspto-grants-2014_09