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Allyl bromide → HCID 14147378, 화합물

HRID 236946
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인쇄 미리보기

반응식

HRID 236946 반응식
[C:1]([C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][C:13]=1[OH:14])[CH2:10][CH2:9][CH2:8][CH2:7]2)(=[O:3])[CH3:2].[CH2:15](Br)[CH:16]=[CH2:17].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[C:1]([C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][C:13]=1[O:14][CH2:17][CH:16]=[CH2:15])[CH2:10][CH2:9][CH2:8][CH2:7]2)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7841Allyl bromideHCID 11430Potassium CarbonateHCID 109432711-(3-Hydroxy-5,6,7,8-tetrahydronaphthalen-2-yl)ethanone

생성물 1

HCID 14147378HCID 14147378, 화합물수율 98.3%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of 6-acetyl-7-hydroxy-1,2,3,4-tetrahydronaphthalene (2.0 g), allyl bromide (1.7 g), anhydrous potassium carbonate (2.2 g) and N,N-dimethylformamide (50 ml) was stirred at room temperature for 24 hours. The mixture was then poured into ice/water (400 ml) and stirred. The precipitate was filtered off, washed with water and then dried to leave, as an off-white powder, 6-acetyl-7-allyloxy-1,2,3,4-tetrahydronaphthalene (2.38 g), mp 62°-63°.

후처리

  1. stirringstirred
  2. filtrationThe precipitate was filtered off
  3. washwashed with water
  4. customdried

출처 및 근거

ORD 기록
ord-204a06a8452e4c6f857cf73276767f8f
출처 데이터셋
uspto-grants-1979_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04159273

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