HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209431Generated: October 26, 2026
Diisopropylamine → 3-Phenyl-2-t-butylcarboxymethylpropionic acid, ethyl ester
https://huagongshe.com/reaction/2209431
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Ethyl 3-phenylpropionate | HCID 16237 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-Phenyl-2-t-butylcarboxymethylpropionic acid, ethyl ester | HCID 86749012 | 46% |
Reaction Steps
Dissolve diisopropylamine (3.5 mL, 25 mmol) in tetrahydrofuran (30 mL). Add n-butyllithium (14 mL of a 1.6M solution in hexane, 22.4 mmol). Stir for 15 minutes and cool to -78° C. Add, by dropwise addition, ethyl dihydrocinnamate (3.5 mL, 20 mmol) and stir for 30 minutes. Add t-butyl bromoacetate (4.0 mL, 25 mmol) and gradually warm to room temperature overnight. Quench the solution with ammonium chloride solution (10 mL) and partition between water (25 mL) and ethyl ether (50 mL). Separate the organic phase, dry (MgSO4) and evaporate the solvent in vacuo. Purify by silica gel chromatography (5% ethyl acetate/hexane) to give 3-phenyl -2-t-butylcarboxymethylpropionic acid, ethyl ester as a pale yellow oil (2.68 g, 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05455242 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-afc23055498143a996f97237774e972b |
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| Source note | uspto-grants-1995_10 |
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