돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42543생성일: 2026년 10월 23일

Potassium Carbonate → 1-(benzyloxymethyl)-2H-tetrazole

https://huagongshe.com/ko/reaction/42543

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Benzyl chloromethyl etherHCID 137983—
반응물HCID 178418441HCID 178418441—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물2-((benzyloxy)methyl)-2H-tetrazoleHCID 1072634044%
생성물1-(benzyloxymethyl)-2H-tetrazoleHCID 6729984547%

반응 단계

A suspension of 1-H-tetrazole (2.0 g, 28.5 mmol) and potassium carbonate (5.9 g, 42.7 mmol) in DMF (30 mL) was treated with benzyl chloromethyl ether (5.36 g, 34.2 mmol), and the reaction mixture was stirred for 4 hours. After this time, the reaction mixture was analyzed by LC/MS, which indicated that the reaction was not complete. As a result, the reaction was treated with benzyl chloromethyl ether (0.5 g, 3.19 mmol) and stirred for about 16 additional hours. At the conclusion of this period, the mixture was filtered, and the filtrate was concentrated in vacuo to yield a residue. The residue was diluted with diethyl ether (200 mL), washed 5× with water (50 mL), once with brine, dried over sodium sulfate, and then concentrated in vacuo. The resulting residue was purified over a 6×20 mm silica gel column, eluting with 20% then 30% ethyl acetate/hexanes to yield 2-(benzyloxymethyl)-2H-tetrazole (2.39 g, 44% yield) and 1-(benzyloxymethyl)-2H-tetrazole (2.56 g, 47% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536198B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-dbce395804984eb8bb043e9523eb5a17
출처 메모uspto-grants-2013_09