2-ethylsulfanylcarbothioylsulfanyl-2-methylpropanoic acid

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: This procedure was adapted from the work of You and Oupický. First, ethanethiol (7.21 mL, 0.1 mol), acetone (73 mL), and tricaprylylmethylammonium chloride (1.0 g, 2.5 mmol) were combined and the mixture was cooled on ice under nitrogen. Next, 9 mL of 50% (w/v) of sodium hydroxide was added dropwise. After an additional 20 minutes, carbon disulfide (6.03 mL, 0.1 mol) and acetone (12.6 mL) were combined and added dropwise. Chloroform (12 mL, 0.15 mol) was added, followed by the addition of 80 mL of 50% (w/v) sodium hydroxide over 10 minutes. The yellow-orange mixture was stirred overnight. Water (200 mL) was added, followed by concentrated hydrochloric acid (80 mL) to drop the pH below 1. The mixture was extracted three times into diethyl ether and concentrated to a dark red oil. Crude product was purified via silica gel chromatography (1:1 hexanes:ether) and then distilled to yield 11.0 g of a bright orange, viscous liquid (49% yield). 1H NMR (CDCl3, δ): 1.33 (t, 3H, —CH2CH3), 1.72 (s, 6H, —C(CH3)2COOH), 3.30 (q, 2H, —CH2CH3). the mixture was cooled on ice under nitrogen added dropwise The mixture was extracted three times into diethyl ether concentrated to a dark red oil Crude product was purified via silica gel chromatography (1:1 hexanes:ether) distilled

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Ethanethiol (7.21 mL, 0.1 mol), acetone (73 mL), and tricaprylylmethylammonium chloride (1.0 g, 2.5 mmol) were combined and cooled on an ice bath under N2. Added 9 mL of 50% (w/v) NaOH to the reaction mixture over 10 minutes. After 20 minutes, carbon disulfide (6.03 mL, 0.1 mol) and acetone (12.6 mL) were combined and added dropwise to the reaction over 30 minutes. Chloroform (12 mL, 0.15 mol) was added, followed by the addition of 80 mL of 50% (w/v) NaOH over 10 minutes. The yellow-orange mixture was stirred overnight. Water (200 mL) was added, followed by concentrated HCl (80 mL) to drop the pH below 1. The mixture was extracted three times into diethyl ether and concentrated to a dark red oil. Crude product was purified via silica gel chromatography (1:1 hexanes:ether) and then distilled to yield 11.0 g of a bright orange, viscous liquid (49% yield). 1H NMR (CDCl3, δ): 1.33 (t, 3H, —CH2CH3), 1.72 (s, 6H, —C(CH3)2COOH), 3.30 (q, 2H, —CH2CH3). cooled on an ice bath under N2 added dropwise to the reaction over 30 minutes The mixture was extracted three times into diethyl ether concentrated to a dark red oil Crude product was purified via silica gel chromatography (1:1 hexanes:ether) distilled