Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Triethylene glycol monomethyl ether | HCID 8178 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131726611 | HCID 131726611 | 12% |
Reaction Steps
Bromoacetic acid tert-butyl ester (20 mL, 0.14 mol), was added over a 10 min period to a rapidly stirred mixture of triethylene glycol monomethyl ether (20 mL, 0.13 mol), tetrabutyl ammonium bromide (20 g, 0.062 mol), toluene (100 mL) and KOH (50% w/w, 100 mL), and the resulting heterogeneous reaction mixture was stirred at 0° C. for 10 min. The reaction mixture was warmed to ambient temperature and stirred for 1 h. Water (100 mL) was added and the organic layer was separated. The organic layer washed with saturated aq. NH4Cl (2×100 mL), saturated aq. NaHCO3 (100 mL), brine (100 mL), and dried over anhydrous MgSO4. The solution was concentrated in vacuo and the residue was loaded onto a silica gel gravity column (200 g) and eluted with ethyl acetate to afford CH3(OCH2CH2)3CH2OCH2CO2C(CH3)3 as a colorless oil (420 g, 12%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07494714B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-41205521d5bb4e0688cb61b94556704f |
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| Source note | uspto-grants-2009_02 |
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