HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223579Generated: October 27, 2026
Acetyl chloride → Methyl (S)-2-benzyloxycarbonylamino-4-oxopentanoate
https://huagongshe.com/reaction/2223579
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | (R)-2-Benzyloxycarbonylamino-3-iodo-propionic acid methyl ester | HCID 10915437 | — |
| Catalyst | Zinc copper couple | HCID 10290809 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Methyl (S)-2-benzyloxycarbonylamino-4-oxopentanoate | HCID 13857370 | — |
Reaction Steps
A mixture of methyl N-((benzyloxy)carbonyl)-3-iodo-L-alaninate (10 g, 27.5 mmol), from Step 1, zinc-copper couple (3.3 g) in benzene (110 mL) and N,N-dimethylacetamide (7.4 mL) was sonicated in an ultra-sound bath for 2 hours. Over this period, 3 portions of 1,2-dibromoethane (0.24 mL) and chlorotrimethylsilane (0.17 mL) were added. To this mixture was then added bis(triphenylphosphine)palladium chloride (0.958 g, 1.4 mmol) and acetyl chloride (2.5 mL, 35.2 mmol) and the mixture was heated at 70° C. for 2 hours. After cooling to room temperature, the mixture was filtered on celite with ethyl acetate, the organic layer was then washed with a saturated solution of ammonium chloride, brine (2×), dried over magnesium sulfate, filtered and the solvent evaporated under vacuum. The residue was purified by silica gel chromatography using ethyl acetate and hexanes to afford methyl N-((benzyloxy)carbonyl)-4-oxo-L-norvalinate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07375134B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-3136d2a640f44ac095b61749af17c96e |
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| Source note | uspto-grants-2008_05 |
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