Methyl iodide → 4,5-Dihydro-3,4,4-trimethyloxazolium iodide

HRID 568916노트

반응식

HRID 568916 반응식
C(C1C=CC(CCCCC2C=CC=CC=2[C:21]2[O:22][CH2:23][C:24]([CH3:27])([CH3:26])[N:25]=2)=CC=1)CCC.[CH3:28][I:29]>>[I-:29].[CH3:28][N+:25]1[C:24]([CH3:27])([CH3:26])[CH2:23][O:22][CH:21]=1

참가 물질

3

반응물 2

HCID 6328Methyl iodideHCID 198479512-[2-(4-(4-Butylphenyl)butyl)phenyl]-4,4-dimethyloxazoline

생성물 1

HCID 118173244,5-Dihydro-3,4,4-trimethyloxazolium iodide

실험 절차

Following the procedures of Example 1(a), (b) and (c), to 4-(4-butylphenyl)butylmagnesium bromide (from 21.47 mmoles of 4-(4-butylphenyl)butyl bromide and 18.96 mmoles of magnesium) in distilled tetrahydrofuran (35 ml) was added 2-(2-methoxyphenyl)-4,4-dimethyloxazoline (16.32 mmoles) in tetrahydrofuran (15 ml). Workup of the reaction mixture furnished 2-[2-(4-(4-butylphenyl)butyl)phenyl]-4,4-dimethyloxazoline as an oil. A solution of the oxazoline (14.41 mmoles) in methyl iodide (20 ml) was refluxed under argon for 18 hours. Removal of the volatiles afforded the corresponding 3,4,4-trimethyloxazolinium iodide as a white solid (mp 91°-94° C.). To an ice cold solution of the iodide (14.07 mmoles) in methanol was added in portions sodium borohydride (14.30 mmoles). Similar treatment of the reaction mixture resulted in the isolation of the desired benzaldehyde product as an oil.

후처리

  1. customRemoval of the volatiles

출처 및 근거

ORD 기록
ord-3d92af277f2b406cbb2912e5a6ba6924
출처 데이터셋
uspto-grants-1988_03
특허 번호
US04730005

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