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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788168Generated: November 5, 2026

2-Thiocresol → (2,2-Diethoxyethyl)(o-tolyl)sulfane

https://huagongshe.com/reaction/1788168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ThiocresolHCID 8712—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
Product(2,2-Diethoxyethyl)(o-tolyl)sulfaneHCID 1061009789%

Reaction Steps

In ethanol (50 mL) was dissolved sodium metal (1.6 g, 66 mmol) at 23° C. 2-Methylbenzenethiol (8.1 mL, 68 mmol) was slowly added to this solution, followed by bromoacetaldehyde diethylacetal (9.50 mL, 63 mmol). The reaction mixture was stirred at reflux for 18 h. The solvent was then evaporated in vacuo and the residue was washed with H2O (100 mL) and extracted with ether (100 mL). The organic solution was dried (MgSO4), concentrated in vacuo and purified by distillation to afford the title compound (13.48 g, 82% yield): 1H NMR (400 MHz, CDCl3) δ ppm: 7.33 (1H, d, J=7.9 Hz), 7.16-7.08 (3H, m), 4.65 (1H, t, J=5.6 Hz), 3.66 (2H, q, J=7.0 Hz), 3.55 (2H, q, J=7.0 Hz), 3.09 (2H, d, J=5.6 Hz), 2.38 (3H, s), 1.20 (6H, t, J=7.0 Hz). LCMS (M+H)+ m/z 241 (t=2.65min.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511037B2
Source datasetuspto-grants-2009_03
ORD IDord-699baf37e77c4cc281afab282509d53b
Source noteuspto-grants-2009_03