HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888352Generated: October 31, 2026
Triethylamine → 2-Benzyloxycarbamoyl-4-methylpentanoic acid ethyl ester
https://huagongshe.com/reaction/1888352
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Benzylhydroxylamine | HCID 2794173 | — |
| Reactant | 2-(Ethoxycarbonyl)-4-methylpentanoic acid | HCID 10103941 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Benzyloxycarbamoyl-4-methylpentanoic acid ethyl ester | HCID 10402138 | 94.5% |
Reaction Steps
Intermediate (3a) (40.3 g, 214 mmol, 1.0 eq) was dissolved into 800 mL DCM and 900 mL THF and the solution was cooled to 0° C. To this was added benzyl hydroxylamine (34.2 g, 214 mmol, 1.0 eq) followed by HOBt (28.9 g, 214 mmol, 1.0 eq). The mixture was stirred for 5 minutes, then DCC (44.1 g, 214 mmol, 1.0 eq) was added, followed by triethylamine (33.4 mL, 240 mmol, 1.1 eq). The mixture was warmed to room temperature and stirred overnight. The solid was filtered and the filtrate was concentrated. The material was redissolved in 1000 mL EtOAc and washed with 500 mL 1N HCl, 600 mL saturated aq. bicarbonate, dried over MgSO4, filtered. and evaporated to yield intermediate (3b) (59.3 g) as a semisolid. MS m/z: [M+H+] calcd for C16H23NO4 294.2. found 294.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501798B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-d685b7da514c457791bf5c62b668595e |
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| Source note | uspto-grants-2013_08 |
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