돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65543생성일: 2026년 10월 24일

6-Bromohexanoic acid → 1-(5-carboxypentyl)-4-(10,15,20-tri-4-pyridyl-21H,23H-porphin-5-yl)pyridinium bromide

https://huagongshe.com/ko/reaction/65543

반응식

참여 물질

역할이름HCID투입량
반응물6-Bromohexanoic acidHCID 20210—
반응물5,10,15,20-Tetra(4-pyridyl)porphyrinHCID 135411729—
용매Chloroform methanolHCID 21584188—
생성물1-(5-carboxypentyl)-4-(10,15,20-tri-4-pyridyl-21H,23H-porphin-5-yl)pyridinium bromideHCID 13633216112.7%

반응 단계

180 mg of 5,10,15,20-tetra(4-pyridyl)-21H,23H-porphine are dissolved in 70 ml of chloroform/methanol (9:1), treated with 585 mg of 6-bromo-caproic acid and subsequently heated at reflux for 20 hours. The solution is then concentrated in vacuo to 5 to 10 ml and the product is precipitated by the addition of 250 ml of ether. The product is added to a 15 cm long silica column, whereupon the elution is carried out with 500 ml of chloroform/methanol (9:1), the starting zone is removed from the column and extracted with 1 liter of methanol and then with 1 liter of chloroform/methanol/water (2:7:1). The material obtained from the extracts is purified further by preparative thick-layer chromatography; eluent: chloroform/methanol/dimethylformamide/water (1:2:1:1). After scratching off, the main zone is extracted twice with 250 ml of methanol each time and twice with 250 ml of chloroform/methanol/water (2:7:1) each time. The product is finally re-precipitated a further four times. For this purpose, it is firstly dissolved in the smallest amount of methanol possible and then precipitated by the slow dropwise addition of 250 ml of chloroform. There are obtained 30 mg of 1-(5-carboxypentyl)-4-(10,15,20-tri-4-pyridyl-21H,23H-porphin-5-yl)pyridinium bromide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04614723
출처 데이터셋uspto-grants-1986_09
ORD IDord-fdfccd3ba46b4460a05b3a357dda990c
출처 메모uspto-grants-1986_09