돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26174생성일: 2026년 10월 25일

Triethylamine → 1-[beta-(2-Methyl-3-indolyl)propionyl]-4-benzyl-4-hydroxypiperidine

https://huagongshe.com/reaction/26174

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물1H-Indole-3-propanoic acid, 2-methyl-HCID 97380—
반응물4-Benzyl-4-piperidinolHCID 98152—
용매ChloroformHCID 6212—
생성물1-[beta-(2-Methyl-3-indolyl)propionyl]-4-benzyl-4-hydroxypiperidineHCID 21324671—

반응 단계

To a stirred solution of 5.0 g of β-(2-methyl-3-indolyl)propionic acid and 2.5 g of triethylamine in 100 ml of chloroform was added dropwise 2.7 g of ethyl chloroformate at a temperature below 0° C. After the addition was complete, stirring was continued for additional 15 minutes and thereto was added 4.7 g of 4-benzyl-4-hydroxypiperidine in several portions. The reaction mixture was stirred for 4 hours at room temperature and allowed to stand overnight. The reaction product was washed thoroughly with water and concentrated to dryness. The residue was recrystallized from ethanol to give 1-[β-(2-methyl-3-indolyl)propionyl]-4-benzyl-4-hydroxypiperidine, melting at 117°-119° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04148796
출처 데이터셋uspto-grants-1979_04
ORD IDord-3024e340990f494fa08720f195cbe64d
출처 메모uspto-grants-1979_04