HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721810Generated: November 2, 2026
1,1'-Carbonyldiimidazole → HCID 54534973, compound
https://huagongshe.com/reaction/1721810
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 3-Methyl-5-isoxazolecarboxylic acid | HCID 76947 | — |
| Reactant | L-Alanine, ethyl ester, hydrochloride (1:1) | HCID 2724356 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54534973 | HCID 54534973 | — |
Reaction Steps
8.2 g of 1,1'-carbonyldiimidazole (CDI) was added to a mixture of 6.35 g of 1B and 75 ml of dry tetrahydrofuran (THF) and the mixture was stirred for 2 hours at room temperature. Then 7.5 g of alanine ethyl ester hydrochloride was added, the mixture was stirred overnight, filtered, and the filtrate was stripped of solvent. The residue was dissolved in 100 ml of a 9:1 v:v mixture of methylene chloride and ethyl acetate, the solution was filtered through silica gel, the gel was washed with 900 ml of the same solvent, then the combined filtrate and washings was stripped of solvent. The residue was a yellow oil that crystallized on standing. The crystals were washed with pentane and dried, to give N-(5-methyl-3-isoxazolylcarbonyl)alanine ethyl ester (1C), as a solid, m.p.: 65°-66° C. 1C was converted to the corresponding acid (1D, a solid, m.p.: 148°-150° C.) in the manner that 1A was converted to 1B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04853027 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-d9fe60ce89734c6b8c6ac535663d4bd5 |
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| Source note | uspto-grants-1989_08 |
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