돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 411261생성일: 2026년 10월 26일

4-Toluenesulfonyl chloride → N-(toluene-4-sulfonyl)-N-methylphenylalanine

https://huagongshe.com/reaction/411261

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물1,4-DioxaneHCID 31275—
반응물N-MethylphenylalanineHCID 6951135—
용매Sodium HydroxideHCID 14798—
생성물N-(toluene-4-sulfonyl)-N-methylphenylalanineHCID 1206925145.6%

반응 단계

N-Methyl-L-phenylalanine (500 mg, 2.79 mmol) was dissolved in 1N NaOH (6 mL). Dioxane (9 mL)) was added, followed by p-toluenesulfonyl chloride (532 mg, 2.79 mmol) and the mixture was vigorously stirred for 1 hr. The volatiles were removed in vacuo and the residue was dissolved in water (30 mL) and washed with Et2O (2×30 mL) before making acidic with 1N HCl. The mixture was extracted with CHCl3 (3×30 mL) and the extracts were evaporated in vacuo to give N-(toluene-4-sulfonyl)-N-methylphenylalanine as a solid (424 mg, 45%). N-(Toluene-4-sulfonyl)-N-methylphenylalanine was coupled to L-phenylalanine ethyl ester using the procedure described in Method 3 (400 mg, 62%). The title compound was prepared via hydrolysis of the ethyl ester using NaOH in ethanol. Proton and carbon NMR analyis indicated a mixture of diastereomers.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06559127B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-f9ebe3facdb3445495e5f2df29712911
출처 메모uspto-grants-2003_05