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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722332Generated: October 30, 2026

Dimethylformamide → 5-Methyl-2-sulfanylbenzaldehyde

https://huagongshe.com/reaction/722332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-MethylbenzenethiolHCID 7811—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantButyllithiumHCID 178418339—
SolventCyclohexaneHCID 8078—
Product5-Methyl-2-sulfanylbenzaldehydeHCID 2188364280.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Tetramethylethylenediamine (TMEDA) (12.6 mL, 83.5 mmol) was added via syringe to n-BuLi (33 mL of 1.6 M in hexanes, 82.5 mmol) and the solution was chilled to 0° C. A solution of p-thiocresol (4.53 g, 36.5 mmol) in cyclohexane (40 mL) was added with stirring over 5 minutes. The resulting tan slurry was stirred overnight at room temperature, chilled to 0° C., and DMF (4.0 mL, 3.77 g, 51.6 mmol) was added via syringe over 2 minutes. The resulting gummy slurry was stirred at room temperature for 1.3 hours. The reaction mixture was added to 3 N HCR (150 mL). This mixture was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated in vacuo yielding a brown oil. This oil was purified by flash chromatography over silica gel, eluting with 10% ethyl acetate-hexanes to afford 5-methyl-2-mercaptobenzaldehyde (4.47 g, 69%) as an intensely yellow solid suitable for use without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138411B2
Source datasetuspto-grants-2006_11
ORD IDord-7de6d122c0184c5395ea7cf1df935205
Source noteuspto-grants-2006_11