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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664173Generated: October 31, 2026

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

https://huagongshe.com/reaction/1664173

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=2.65 min.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039458B2
Source datasetuspto-grants-2011_10
ORD IDord-58af464f6b0a44979391397d22e29313
Source noteuspto-grants-2011_10