HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405031Generated: October 25, 2026
Lithium Bromide → Methyl (S)-2-benzyloxycarbonylamino-4-oxo-5-phenylpentanoate
https://huagongshe.com/reaction/405031
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | Methyl (S)-2-benzyloxycarbonylamino-3-chlorocarbonylpropionate | HCID 11055664 | — |
| Reactant | HCID 178418336 | HCID 178418336 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl (S)-2-benzyloxycarbonylamino-4-oxo-5-phenylpentanoate | HCID 57535346 | 53.1% |
Reaction Steps
To a suspension of copper(I) bromide-dimethyl sulfide complex (2.6 g, 12.72 mmol, 1.2 eq.) in dry THF was added a solution of lithium bromide (2.2 g, 25.44 mmol, 2.4 eq.) in dry THF. The mixture was stirred at room temperature (RT) for 20 min, and then was cooled to −78° C. A solution of benzyl magnesium chloride (13 mL, 12.72 mmol, 1.2 eq.) followed by a solution of (S)-methyl 2-(benzyloxycarbonylamino)-4-chloro-4-oxobutanoate (3.16 g, 10.6 mmol, 1 eq.) in dry THF were added. The mixture was stirred at −78° C. for 30 min and then was quenched with sat. ammonium chloride. The mixture was extracted with ethyl acetate. The organic layers were dried over magnesium sulfate and then concentrated in vacuo. The residue was purified by flash column (1:1 ethyl acetate:hexane) to give 2 g of (S)-methyl 2-(benzyloxycarbonylamino)-4-oxo-5-phenylpentanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748649B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-8653999278ee4bb7ac3598bbcf43c7af |
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| Source note | uspto-grants-2014_06 |
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