Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223320Generated: October 31, 2026

Ethane, 2-bromo-1,1-diethoxy- → HCID 59715279, compound

https://huagongshe.com/reaction/2223320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
ReactantSodium ethoxideHCID 2723922—
Reactant14395-51-8HCID 19921798—
SolventEthanolHCID 702—
ProductHCID 59715279HCID 5971527988%

Reaction Steps

To a solution of the thiocarbamic acid S-ester (34.7 g) in THF (500 mL) under an atmosphere of nitrogen was added a solution of KOH (17.8 g, 2.5 equiv) in MeOH (90 mL), the solution allowed to stir at room temperature for 5 hr and quenched by the addition of 1N HCl, extracted with EtOAc and the organic phase was washed with brine, dried over Na2SO4, filtered and concentrated to give 4-bromo-2-methyl benzenethiol which was used immediately. The thiol was added dropwise to a solution of sodium ethoxide (10.3 g, 1.2 equiv) in EtOH (600 mL), allowed to stir for 30 min before the dropwise addition of 2-bromo-1,1-diethoxyethane (23 mL, 1.2 equiv). The reaction mixture was heated at reflux for 4 hr, allowed to cool and stir at room temperature overnight, then quenched by the addition of water and concentrated. Water and EtOAc were added, the phases separated, and the aqueous phase was further extracted with EtOAc. The organic phase was dried over Na2SO4, filtered and concentrated. The crude product was purified by column chromatography (SiO2, 5% EtOAC in hexanes) to give 4-bromo-1-(2,2-diethoxyethylsulfanyl)-2-methylbenzene (38.4 g, 88% for 2 steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375125B2
Source datasetuspto-grants-2008_05
ORD IDord-431b16abea744cc0948c7cde4e2623bb
Source noteuspto-grants-2008_05