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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 381393생성일: 2026년 10월 26일

5-Phenyl-1-pentanol → Benzenepentanal

https://huagongshe.com/reaction/381393

반응식

참여 물질

역할이름HCID투입량
반응물5-Phenyl-1-pentanolHCID 61523—
반응물Sodium BromideHCID 253881—
반응물Sodium BicarbonateHCID 516892—
반응물TempoHCID 2724126—
반응물Sodium HypochloriteHCID 23665760—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물BenzenepentanalHCID 561886—

반응 단계

A vigorously stirred solution of 5-phenylpentanol (10 g), sodium bromide (6.45 g) and TEMPO, 2,2,6,6-tetramethyl-1-piperidinyloxy, (0.095 g) in a mixture of ethyl acetate, toluene and water (258 ml, 7:7:1, v/v/v), at 0° C., was treated with aqueous sodium hypochlorite solution (571 ml, 0.35M) saturated with sodium bicarbonate (43.85 g) in five portions separated by 10 minute intervals. The reaction mixture was treated with ethanol (20 ml) then partitioned between water (500 ml) and ethyl acetate (500 ml). The aqueous layer was extracted twice with ethyl acetate (500 ml). The combined organic phases were washed with aqueous sodium thiosulphate (500 ml, 5%), then with water (200 ml), then with brine (200 ml), then dried over magnesium sulphate and then evaporated to give the title compound as an orange oil, which was used without further purification. NMR (CDCl3): δ1.65 (m,4H), 2.35 (m,2H), 2.60 (t,2H), 7.10-7.30 (m,5H), 9.75 (s,1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06306873B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-90ac1b90566c4670ac0d425ee9a63bf3
출처 메모uspto-grants-2001_10