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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721224Generated: November 3, 2026

HCID 14913644, compound → HCID 178519098, compound

https://huagongshe.com/reaction/1721224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14913644HCID 14913644—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178478438HCID 178478438—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 178519098HCID 178519098—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To 6.8 g of 3-trityl-2,4-oxazolidinedione dissolved in 200 ml of tetrahydrofuran were added 13.6 ml of n-butyllithium and, after 15 minutes of stirring at -78° C., 3.9 g of trans-1,4-bis[(4-chloromethylphenoxy)methyl]cyclohexane which has been dissolved in 20 ml of tetrahydrofuran, followed by additional 2 hours of stirring at -78° C. After completion of the reaction, the reaction mixture was dispersed in saturated ammonium chloride aqueous solution and ice layers and extracted with ethyl acetate. The ethyl acetate layer was washed with saturated sodium chloride aqueous solution, dried over anhydrous sodium sulfate and then evaporated to dryness, thereby obtaining crude trans-1,4-bis[[4-[(3-trityl-2,4-dioxo-5-oxazolidinyl)methyl]phenoxy]methyl]cyclohexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508296
Source datasetuspto-grants-1996_04
ORD IDord-c19fb9435780457290ef1423b1a9be70
Source noteuspto-grants-1996_04