HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230434Generated: November 1, 2026
Dimethyl Sulfoxide → t-Butyl N-Allyloxycarbonyl-4-amino-5-oxopentanoate
https://huagongshe.com/reaction/2230434
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | t-Butyl N-allyloxycarbonyl-4-amino-5-hydroxypentanoate | HCID 18465850 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | t-Butyl N-Allyloxycarbonyl-4-amino-5-oxopentanoate | HCID 18465646 | — |
Reaction Steps
To a solution of DMSO (1.51 g, 19.3 mmol) in CH2Cl2 (25 ml) at −70° C. was added oxalyl chloride (1.34 g, 19.3 mmol). After 10 minutes at −70° C., a solution of (206a) (2.4 g, 8.8 mmol) in CH2Cl2 (10 ml) was added dropwise and the mixture stirred for 15 minutes at −70° C. Diisopropylethylamine (3.4 g, 26.3 mmol) was added and the mixture stirred at −25° C. for 15 minutes then diluting with EtOAc (50 ml) washed with a solution of sodium hydrogen sulfate 2M, concentrated to give an oil which was used immediately without purification: 1H NMR (CDCl3) δ9.5 (1H, s), 6.0-5.5 (2H, m), 5.5-5.1 (2H, m), 4.5 (2H, m), 4.2 (1H, m), 2.4-2.10 (2H, m), 2.05 (2H, m), 1.36 (9H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06423840B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-72c7b77761624d43be748fab8fcdeec4 |
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| Source note | uspto-grants-2002_07 |
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