HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771022Generated: November 1, 2026
Hydrochloric Acid → t-butoxycarbonylmethyl 5-(Boc-amino)-4-oxopentanoate
https://huagongshe.com/reaction/1771022
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | 5-((tert-Butoxycarbonyl)amino)-4-oxopentanoic acid | HCID 17989820 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | t-butoxycarbonylmethyl 5-(Boc-amino)-4-oxopentanoate | HCID 90034544 | 89% |
Reaction Steps
Triethylamine (2.22 g; 22.0 mmol) was added dropwise to a stirred solution of 5-(Boc-amino)-4-oxopentanoic acid (4.62 g; 20.0 mmol) and t-butyl bromoacetate (4.30 g; 22.0 mmol) in ethyl acetate (60 mL) under argon at ambient temperature. The mixture (slurry) was refluxed for 17 h, then cooled to ambient temperature, poured into 0.5 M HCl (100 mL) and shaken thoroughly. The aqueous portion was extracted with ethyl acetate (2×20 mL). The combined organic solutions were washed with saturated NaHCO3 solution (1×20 mL) and saturated NaCl solution (1×20 mL) then dried (MgSO4), filtered and evaporated. Evaporation resulted in an amber oil that was purified by flash chromatography on a 40×55-mm silica gel 60 column eluted with ethyl acetate-hexane (1:1) (600 mL), collecting 5×100 mL fractions. Evaporation of fractions 1 and 2 resulted in 6.15 g (89%) product (yellow oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249086B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-043ee78e928c4da7b67a8a64d9a49c80 |
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| Source note | uspto-grants-2016_02 |
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