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HRID 26327作成日:2026年10月24日

L-Alanine → N-((1,1-Dimethylethoxy)carbonyl)-L-alanyl-L-alanine

https://huagongshe.com/ja/reaction/26327

反応式

関与物質

役割名称HCID仕込み量
反応物L-AlanineHCID 5950—
反応物4-MethylmorpholineHCID 7972—
反応物Boc-Ala-OSuHCID 11011585—
溶媒DimethylformamideHCID 6228—
生成物N-((1,1-Dimethylethoxy)carbonyl)-L-alanyl-L-alanineHCID 6992569—

反応手順

L-Alanine (3.57 g, 40 mmol) was dissolved in 18.8 ml of Triton B (40 mmol), evaporated to dryness, and the oily residue re-evaporated twice with DMF (30 ml each). The salt obtained was stirred with 11.45 g of Boc-Ala-OSu (40 mmol) in 40 ml DMF, with 4 ml of NMM added, for 20 hours. The solvent was removed and the residue taken up in 10% HOAc (100 ml). The product was extracted into EtOAc (4 times 100 ml), washed twice with a small volume of H2O, dried over Na2SO4, evaporated to a small volume, and treated with petroleum ether until cloudiness developed. A crystalline product formed on storage in the refrigerator overnight: Yield, 8.2 g (76.3%); mp 115°-118°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04148788
出典データセットuspto-grants-1979_04
ORD IDord-9889250ba2dc449bb2d7d2a9635c9889
出典メモuspto-grants-1979_04