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Potassium Carbonate → 3-[3-(Hydroxymethyl)benzylthio]benzaldehyde

HRID 2254476
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반응식

HRID 2254476 반응식
[SH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6].[OH:10][CH2:11][C:12]1[CH:13]=[C:14]([CH:17]=[CH:18][CH:19]=1)[CH2:15]Br.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[OH:10][CH2:11][C:12]1[CH:13]=[C:14]([CH:17]=[CH:18][CH:19]=1)[CH2:15][S:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 149468343-SulfanylbenzaldehydeHCID 19032333(3-(Bromomethyl)phenyl)methanol

생성물 1

HCID 197446443-[3-(Hydroxymethyl)benzylthio]benzaldehyde수율 51%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

200 mg of 3-mercaptobenzaldehyde was dissolved in 6 ml of dimethylformamide, and 291 mg of 3-hydroxymethylbenzyl bromide and 402 mg of potassium carbonate were added. The mixture was stirred for 3 hours at room temperature. The solvent was evaporated, water and ethyl ether were added to the residue to extract it. The extract was worked up in a customary manner, and purified by silica gel column chromatography [Wakogel C-200, 10 g; eluting solvent: hexane/ethyl acetate=2/1] to give 190 mg (yield 51%) of 3-[3-(hydroxymethyl)benzylthio]benzaldehyde as a pale yellow oil.

후처리

  1. customThe solvent was evaporated
  2. additionwater and ethyl ether were added to the residue
  3. extractionto extract it
  4. custompurified by silica gel column chromatography [Wakogel C-200, 10 g; eluting solvent: hexane/ethyl acetate=2/1]

출처 및 근거

ORD 기록
ord-a4446670440348fe8319cf2be265b890
출처 데이터셋
uspto-grants-1993_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05234946

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