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Triphenylphosphine → 3-(5-Bromopentyl)-5-methylisoxazole

HRID 2165386
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HRID 2165386 반응식
O[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]1[CH:11]=[C:10]([CH3:12])[O:9][N:8]=1.BrBr.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CC1ON=C(CCC[Br:43])C=1>>[Br:43][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]1[CH:11]=[C:10]([CH3:12])[O:9][N:8]=1
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참가 물질

5

반응물 4

HCID 11776TriphenylphosphineHCID 24408BromineHCID 133169753-(3-Bromopropyl)-5-methyl-1,2-oxazoleHCID 133169773-(5-Hydroxypentyl)-5-methylisoxazole

생성물 1

HCID 133169783-(5-Bromopentyl)-5-methylisoxazole수율 77%

실험 절차

3-(5-Bromopentyl)-5-methylisoxazole [XXVII; R9 =CH3, Hal=Br] was prepared by reacting 3-(5-hydroxypentyl)-5-methylisoxazole with bromine and triphenylphosphine according to the procedure of part (f) above, and was obtained in 77% yield as an oil, b.p. 140°-150° C.(0.05 mm).

후처리

  1. customwas obtained in 77% yield as an oil, b.p. 140°-150° C.(0.05 mm)

출처 및 근거

ORD 기록
ord-259b03d39dd64db6a99067f99b130b55
출처 데이터셋
uspto-grants-1990_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04939267

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