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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899277Generated: October 29, 2026

HCID 22640688, compound → HCID 22640670, compound

https://huagongshe.com/reaction/899277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22640688HCID 22640688—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22640670HCID 22640670—

Reaction Steps

A suspension of methyl triphenylphosphonium bromide (2.293 g, 6.42 mmole) in 40 mL of THF at 0° C., was treated dropwise with 2.6 mL of 2.5M butyllithium. The mixture was stirred at room temperature for 30 minutes and then cooled to 0° C. A solution of 1-(4,4-dimethyl-thiochroman-7-yl)-hexan-1-one (1.183 g, 4.28 mmole) in 10 mL of THF was added to the ylide solution. The reaction mixture was stirred at room temperature for one hour, quenched by the addition of 50 mL water and was extracted with three 50 mL portions of ether. The combined organic extracts were dried over MgSO4, filtered and concentrated in vacuo to give a yellow solid. The product was purified by flash chromatography (SiO2, 1% ethyl acetate in hexanes) to yield 0.939 g of 4,4-dimethyl-7-(1-methylene-hexyl)-thiochroman as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07354931B2
Source datasetuspto-grants-2008_04
ORD IDord-7b7047c965a244f2921f3fcb732cd5d7
Source noteuspto-grants-2008_04