HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644180Generated: October 29, 2026
Triphenylphosphine → methyl 4-(tert-butyl)-2-(1-Boc-piperidin-4-yloxy)benzoate
https://huagongshe.com/reaction/644180
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | — |
| Reactant | Methyl 4-tert-butyl-2-hydroxybenzoate | HCID 20777194 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl 4-(tert-butyl)-2-(1-Boc-piperidin-4-yloxy)benzoate | HCID 68532357 | 73% |
Reaction Steps
To a stirring solution of methyl 4-tert-butyl-2-hydroxybenzoate (9.45 g, 45.4 mmol), 1-Boc-piperidine-4-ol (9.6 g, 47.7 mmol) and triphenylphosphine (12.5 g, 47.7 mmol) in THF (125 mL) was added, dropwise via an addition funnel, a solution of diisopropyl azodicarboxylate (9.4 mL, 47.7 mmol) in THF (25 mL). After 72 h, the solvent was removed in vacuo and the residue was dissolved in a minimal amount of chloroform and vacuum filtered through a pad of silica gel, eluting with a solution of 20% ethyl acetate in hexanes. The filtrate was then concentrated in vacuo and the residue was chromatographed over silica gel, eluting with a gradient of 5% ethyl acetate in hexanes through 20% ethyl acetate in hexanes. The product containing fractions were combined and concentrated in vacuo to give 12.9 g (73% of a thick colorless oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700628B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-0429d96806a04c05924b2cac571083cc |
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| Source note | uspto-grants-2010_04 |
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