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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409669Generated: October 28, 2026

Ethyl Acetate → HCID 86625459, compound

https://huagongshe.com/reaction/409669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSulfuryl chlorideHCID 24648—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 69181575HCID 69181575—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86625459HCID 86625459—

Reaction Conditions

Temperature-15 °C

Reaction Steps

A solution of sulfurylchloride (0.92 ml, 11.0 mmol, 1.16 equiv) in DCM (20 mL) is added dropwise (30 min) to a cold (−15° C.) solution of (2-iodo-3,5-dimethoxy-phenyl)-carbamic acid tert-butyl ester (3.6 g, 9.49 mmol) in THF (48 ml), under an argon atmosphere. The reaction mixture is allowed to stir for 1 h at −15° C. and then poured onto a mixture of ice/H2O (100 mL), a saturated aqueous solution of NaHCO3 (80 ml), and EtOAc (100 mL). The layers are separated and the aqueous phase is extracted with EtOAc (2×100 mL). The combined organic phase is washed with H2O (3×60 mL) and brine (60 mL), dried (Na2SO4), filtered and concentrated. The residue is purified by silica gel column chromatography (DCM) followed by crystallization from DCM/Hex to afford the title compound. ESI-MS: 411.9, 413.9 [M-H]+, TLC: Rf=0.18 (DCM/Hex, 7:3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759517B2
Source datasetuspto-grants-2014_06
ORD IDord-d941c9a2a37c452c8b0285b2e267b502
Source noteuspto-grants-2014_06