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Formaldehyde → 2,6-Diethyl-4-methylbenzyl alcohol

HRID 385239
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인쇄 미리보기

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HRID 385239 반응식
[CH2:1]=[O:2].[CH2:3]([C:5]1[CH:10]=[C:9]([CH3:11])[CH:8]=[C:7]([CH2:12][CH3:13])[C:6]=1[Mg]Br)[CH3:4].BrC1C(CC)=CC(C)=CC=1CC.[Mg]>C1COCC1>[CH2:3]([C:5]1[CH:10]=[C:9]([CH3:11])[CH:8]=[C:7]([CH2:12][CH3:13])[C:6]=1[CH2:1][OH:2])[CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 712FormaldehydeHCID 5462224MagnesiumHCID 115794912-Bromo-1,3-diethyl-5-methylbenzeneHCID 178436244HCID 178436244, 화합물

생성물 1

HCID 667075402,6-Diethyl-4-methylbenzyl alcohol수율 71%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Over a period of 30 min, gaseous formaldehyde (generated from 5.56 g of paraformaldehyde) is introduced with stirring into a solution of 2,6-diethyl-4-methylphenylmagnesium bromide, prepared from 12.40 g (54.6 mmol) of 1-bromo-2,6-diethyl-4-methylbenzene and 1.47 g (60.65 mmol) of magnesium turnings in 50 ml of THF, and the mixture is then stirred at room temperature for another 2 h. Distillative removal of the solvent and chromatography on silica gel (see above) gives 6.88 g (71%) of 2,6-diethyl-4-methylbenzyl alcohol.

후처리

  1. customDistillative removal of the solvent and chromatography on silica gel (see above)

출처 및 근거

ORD 기록
ord-c31da7488e184db396b4480431eb0d6a
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08367873B2

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