HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471445Generated: October 30, 2026
Triphenylphosphine → HCID 86703885, compound
https://huagongshe.com/reaction/471445
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Bromo-3,5-dimethylphenol | HCID 81970 | — |
| Reactant | Di-tert-butyl diazene-1,2-dicarboxylate | HCID 6034084 | — |
| Reactant | 1427028-11-2 | HCID 57578793 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86703885 | HCID 86703885 | — |
Reaction Steps
4-bromo-3,5-dimethylphenol, (306 mg, 1.52 mmol), (1-Methanesulfonyl-cyclopropyl)-methanol (228 mg, 1.52 mmol), and triphenylphosphine (399 mg, 1.52 mmol) are suspended in dry tetrahydrofuran (10 mL) and cooled to 0° C. Di-tert-butylazodicarboxylate (350 mg, 1.52 mmol) is added and the mixture stirred at 50° C. for 48 hours then at room temperature for a further 48 hours. The mixture is concentrated under vacuum then partitioned between water and dichloromethane, The organic phase is dried and the solvent removed under vacuum. The residue is purified by flash chromatography (0-20% ethyl acetate in cyclohexane) to give the title compound as a crude material which was used without further purification (Yield 664 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633182B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-39753b914b4b445ab38229b114cac4de |
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| Source note | uspto-grants-2014_01 |
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