Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016246Generated: October 30, 2026

HCID 11265458, compound → HCID 11436844, compound

https://huagongshe.com/reaction/1016246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11265458HCID 11265458—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11436844HCID 11436844—

Reaction Steps

At 0° C., potassium tert-butoxide (6.2 g, 55.4 mmol) was added to a solution of methyltriphenylphosphonium bromide (19.7 g, 55.4 mmol) in THF (180 ml). At from −10 to −5° C., 3-bromo-2-methoxy-6-methylsulfanylbenzaldehyde (12 g, 46 mmol) dissolved in THF (180 ml) was then added, and the mixture was stirred overnight at RT for 7 h. The mixture was filtered, and the solution was admixed with H2O (200 ml) and MTBE (200 ml) and then extracted with MTBE (200 ml). The combined organic phases were dried over MgSO4 and concentrated. Chromatography (cyclohexanez→cyclohexane/EtOAc 9:1) gave 1-bromo-2-methoxy-4-methylsulfanyl-3-vinylbenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06475957B1
Source datasetuspto-grants-2002_11
ORD IDord-586c592d79bc4859bedd3e38f726aeba
Source noteuspto-grants-2002_11