HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721224Generated: November 3, 2026
HCID 14913644, compound → HCID 178519098, compound
https://huagongshe.com/reaction/1721224
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 14913644 | HCID 14913644 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178478438 | HCID 178478438 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 178519098 | HCID 178519098 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05508296 |
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| Source dataset | uspto-grants-1996_04 |
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| ORD ID | ord-c19fb9435780457290ef1423b1a9be70 |
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| Source note | uspto-grants-1996_04 |
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