HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383894Generated: October 25, 2026
Triphenylphosphine → HCID 22949959, compound
https://huagongshe.com/reaction/1383894
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | Benzenepropanoic acid, 4-hydroxy-, methyl ester | HCID 79706 | — |
| Reactant | Dodecyl(2-hydroxyethyl)methylamine | HCID 10657884 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22949959 | HCID 22949959 | 887.5% |
Reaction Steps
A solution of methyl 3-(4-hydroxyphenyl)propionate (10.0 g, 55. 5 mmol), N-methyl-N-dodecylethanolamine (13.5 g, 55.5 mmol) and triphenylphosphine (16.0 g, 61.0 mmol) in dry tetrahydrofuran (200 ml) was treated at 22° C. with diisopropyl azodicarboxylate (12.3 g, 61.0 mmol) added dropwise over 50 min. After 3 h at 22° C., the reaction mixture was evaporated under reduced pressure and the residue was triturated with hexane. The solid formed was filtered, washed with hexane and the combined filtrate was chromatographed on silica gel using a gradient of ethyl acetate in hexane (20%-60%) as eluent. Distillation under vacuum then gave 18.0 g (75%) of 3-{4-[2-(N-dodecyl-N-methylamino)ethoxy]phenyl} propanoic acid, methyl ester as a clear oil: b.p. 180-183° C./0.02 torr (bulb to bulb distillation, air bath temperature).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06255496B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-a6db91919c714284aa39326dd7778a41 |
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| Source note | uspto-grants-2001_07 |
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