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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 863595생성일: 2026년 10월 24일

Triphenylphosphine → 3-[4-(2-Methyltetrazol-5-yl)-2,6-dimethylphenoxy]-propylbromide

https://huagongshe.com/ko/reaction/863595

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물3-Bromo-1-propanolHCID 12308—
반응물Win 58768HCID 148372—
반응물Diethyl azodicarboxylateHCID 5462977—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물3-[4-(2-Methyltetrazol-5-yl)-2,6-dimethylphenoxy]-propylbromideHCID 1539152382%

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온도0 °C

반응 단계

A mixture of (3-hydroxypropyl)-bromide (2.17 ml, 24 mmol), 4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenol (5.1 g, 25 mmol), and DEAD (4.18 g, 24 mmol) was dissolved in 50 ml of THF at 0° C. To the above solution was added dropwise triphenylphosphine (6.3 g, 24 mmol) at 0° C. and the mixture was allowed to stir at 0° C. for 0.5 h. The mixture was diluted with 500 ml of water and 100 ml of ether, and the aqueous layere was extracted with ether (2×400 ml). The combined organic layer was dried over sodium sulfate, and concentrated in vacuo. The residue was dissolved in 800 ml of ether, and the organic layer was washed with 10% NaOH solution (3×50 ml), dried over sodium sulfate, and concentrated in vacuo. The residue was purified by silica column chromatography (7 cm column, ethyl acetate/hexane, 1/5) followed by recrystallization from methylene chloride/hexane to afford 6.4 g (82%) of 3-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-propylbromide, as a light yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05721261
출처 데이터셋uspto-grants-1998_02
ORD IDord-792e706ecee04535a5e151d198656c3c
출처 메모uspto-grants-1998_02