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Bromine → 5-Bromo-2-hydroxy-3-methylbenzaldehyde

HRID 855097
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반응식

HRID 855097 반응식
[OH:1][C:2]1[C:9]([CH3:10])=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].[Br:11]Br>C(O)(=O)C.O>[Br:11][C:7]1[CH:8]=[C:9]([CH3:10])[C:2]([OH:1])=[C:3]([CH:6]=1)[CH:4]=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24408BromineHCID 5227773-Methylsalicylaldehyde

생성물 1

HCID 27570165-Bromo-2-hydroxy-3-methylbenzaldehyde수율 88.6%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매

실험 절차

The solution of 2-Hydroxy-3-methylbenzaldehyde (1.0 g, 7.35 mmole) in acetic acid (6 mL) was cooled to 0° C. (ice bath). Bromine (1.36 g, 8.52 mmole) was added dropwise and allowed to stir for 2 hours. The reaction was warmed to room temperature and diluted with water (100 mL) yielding a light orange precipitate. The solid was filtered and washed with water (10 mL). Dried on high vacuum to give a light brown solid (1.4 g, 88.6%). 1H NMR (CDCl3/400 MHz) 11.16 (s, 1H), 9.79 (s, 1H), 7.48 (s, 1H), 7.46 (s, 1H), 2.23 (s, 3H).

후처리

  1. customyielding a light orange precipitate
  2. filtrationThe solid was filtered
  3. washwashed with water (10 mL)
  4. customDried on high vacuum

출처 및 근거

ORD 기록
ord-2129189d30cf43e9beacb6550c373296
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07259266B2

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