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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979555Generated: October 31, 2026

Potassium Carbonate → (2,2-Diethoxyethyl)(3-methoxyphenyl)sulfane

https://huagongshe.com/reaction/979555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
Reactant3-MethoxybenzenethiolHCID 84989—
SolventAcetoneHCID 180—
Product(2,2-Diethoxyethyl)(3-methoxyphenyl)sulfaneHCID 1364251697.2%

Reaction Steps

Bromoacetaldehyde diethyl acetal (16.5 ml, 0.11 mol) was added dropwise to a mixture of m-methoxybenzenethiol (15.0 ml, 0.12 mol) and K2CO3 (16.6 g, 0.12 mol) in acetone (150 ml) at room temperature. The reaction mixture was stirred for 16 hours and then filtered. The solid was washed with acetone, and the combined filtrate and washes were concentrated in vacuo. The residue was diluted with H2O and extracted with Et2O. The Et2O extracts were washed with 0.5 M KOH, H2O, and brine, dried over Na2SO4, filtered, and concentrated in vacuo to give 27.4 g of 1-[(2,2-diethoxy)ethylthio]-3-methoxybenzene as a dark yellow oil. 'H NMR, δ :(CDCl3):1.18 (6H, t, --OCHHD 2CH3); 3.13 (2H, d, --SCH--); 3.43-3.73 (4H, m, --OC/H/ 2CH3); 3.77 (3H, s, --OCH 3); 4.67 (1H, t, --SCH2C/H/ --); 6.60-7.27 (4H, m, aromatics).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04668697
Source datasetuspto-grants-1987_05
ORD IDord-69f1a76d35ea4ed3b16c6cb39b1c8c78
Source noteuspto-grants-1987_05