HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497545Generated: October 30, 2026
Glycine tert-butyl ester → HCID 90281924, compound
https://huagongshe.com/reaction/1497545
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycine tert-butyl ester | HCID 151417 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | tert-Butyl (3-formylphenoxy)acetate | HCID 14971816 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 90281924 | HCID 90281924 | 52.9% |
Reaction Steps
To a solution of tert-butyl (3-formylphenoxy)acetate (1.50 g) in dichloroethane (20.0 mL) were added tert-butyl glycinate (874 mg) and acetic acid (1.09 mL), and then sodium triacetoxyborohydride (2.69 g) was added thereto under ice-cooling. The reaction suspension was stirred at room temperature for 16 hours. To the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform-methanol) to obtain tert-butyl N-[3-(2-tert-butoxy-2-oxoethoxy)benzyl]glycinate (1.18 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199927B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-822cc138dfc34e33bbf1060376a1bfef |
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| Source note | uspto-grants-2015_12 |
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