HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296968Generated: November 3, 2026
Triphenylphosphine → (S)-[3-(2-Methyl-3-bromopropoxy)phenyl]acetic acid methyl ester
https://huagongshe.com/reaction/1296968
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Methyl 3-Hydroxyphenylacetate | HCID 39129 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | (S)-(+)-3-Bromo-2-methyl-1-propanol | HCID 10986449 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (S)-[3-(2-Methyl-3-bromopropoxy)phenyl]acetic acid methyl ester | HCID 57757118 | 63.5% |
Reaction Steps
To a stirring solution of (3-hydroxy-phenyl)-acetic acid methyl ester (0.75 g, 0.0045 mol) in anhydrous toluene (30 mL) was added (S)-(+)-3-bromo-2-methyl-1-propanol (0.90 g, 0.0059 mol). Polymer bound triphenylphosphine (2.4 g, 0.0072 mole, 3 mmol/g, Fluka Chemie) was then added, and the mixture was stirred for 15 minutes. The reaction mixture was then cooled to 0° C. and diisopropylazodicarboxylate (1.1 g, 0.0056 mol) was added in a dropwise fashion. After stirring at room temperature overnight, the crude reaction mixture was filtered, and the solid washed with toluene. After concentration of the filtrate in vacuo, the crude product was purified by column chromatography over silica gel (silica gel 60, EM Science) using 15% EtOAc:hexane as eluent to afford 0.86 g (63% yield) of the title compound as an oil: MS (ESI) 303.0 (M+2H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07247748B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-f208aa8f276a4b91ba86875cdb0e9be3 |
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| Source note | uspto-grants-2007_07 |
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