HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353168Generated: November 1, 2026
Triethylamine → Methyl 2-{[4-(2-tert-butoxy-1,1-dimethyl-2-oxoethoxy)benzyl]amino}butyrate
https://huagongshe.com/reaction/353168
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Alpha-aminobutyrate | HCID 21889526 | — |
| Reactant | tert-Butyl 2-(4-formylphenoxy)-2-methylpropanoate | HCID 22708193 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | Methyl 2-{[4-(2-tert-butoxy-1,1-dimethyl-2-oxoethoxy)benzyl]amino}butyrate | HCID 22708231 | 89% |
Reaction Steps
Similarly to the procedure of Example I-5, 1.20 g (4.54 mmol) of tert-butyl 2-(4-formylphenoxy)-2-methylpropionate (Example I-4) and 0.70 g (4.54 mmol) of methyl DL-2-aminobutyrate are reacted at room temperature with 0.92 g (9.08 mmol) of triethylamine and 1.44 g (6.81 mmol) of sodium triacetoxyborohydride in 10 ml of dichloroethane. A further 0.9 g (4.25 mmol) of sodium triacetoxyborohydride and 0.35 g (2.27 mmol) of methyl DL-2-aminobutyrate are added and the mixture is heated at 40° C. for 3 h, giving 1.47 g (89%) of methyl 2-{[4-(2-tert-butoxy-1,1-dimethyl-2-oxoethoxy)benzyl]amino}butyrate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06750236B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-17eff5b5aead423fb02c1818a0dd98d7 |
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| Source note | uspto-grants-2004_06 |
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