HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444678Generated: November 2, 2026
Tributylstannane → BENZYL 4-OXO-2-[[(PHENYLMETHOXY)CARBONYL]AMINO]BUTANOATE
https://huagongshe.com/reaction/1444678
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Z-Asp-OBzl | HCID 6994509 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | BENZYL 4-OXO-2-[[(PHENYLMETHOXY)CARBONYL]AMINO]BUTANOATE | HCID 11359778 | — |
Reaction Steps
To a solution of Z-Asp-OBn (10 g, 0.028 mol) in MC (200 ml), oxalyl chloride (2.93 ml, 0.0336 mol) and a catalytic amount of DMF were added at 0° C. and stirred at room temperature for 2 hrs. After the solvent was evaporated, the crude acyl chloride was dissolved in benzene (400 ml), and tributyltin hydride (15.1 ml, 0.056 mol) and a catalytic amount of Pd(0) were added slowly at 0° C. and stirred at room temperature overnight. After the solvent was evaporated, ether (100 ml)/10% KF in water (100 ml) was added and stirred at room temperature for 2 hrs, followed by filtration to give a biphasic solution. The organic layer was separated and concentrated to give a crude product, which was purified by column chromatography to obtain the title compound, Z-Asp-OBn aldehyde (6 g) as pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662960B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-94edc024db3f49ccad71ef43ff1c1247 |
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| Source note | uspto-grants-2010_02 |
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