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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 57506022, 화합물

HRID 1942713
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HRID 1942713 반응식
[Br:1][C:2]1[C:3]([CH2:14][CH3:15])=[C:4]([CH:8]([OH:13])S([O-])(=O)=O)[CH:5]=[CH:6][CH:7]=1.Cl>C1COCC1>[Br:1][C:2]1[C:3]([CH2:14][CH3:15])=[C:4]([CH:5]=[CH:6][CH:7]=1)[CH:8]=[O:13]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 86659011HCID 86659011, 화합물

생성물 1

HCID 57506022HCID 57506022, 화합물수율 81.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of (3-bromo-2-ethylphenyl)(hydroxy)methanesulfonate (5.26 g, 16.59 mmol) in THF (25 mL) was added HCl (16.59 mL, 49.8 mmol). The mixture was stirred for an hour at rt. THF was removed under the reduced pressure. Residue was dissolved in EtOAc (50 mL) then washed with brine (10 mL). The organic phase was dried over anhydrous sodium sulfate, concentrated under the reduced pressure and dried in vacuum to give 3-bromo-2-ethylbenzaldehyde (2.89 g) as pale yellow oil.

후처리

  1. customTHF was removed under the reduced pressure
  2. dissolutionResidue was dissolved in EtOAc (50 mL)
  3. washthen washed with brine (10 mL)
  4. dry with materialThe organic phase was dried over anhydrous sodium sulfate
  5. concentrationconcentrated under the reduced pressure
  6. customdried in vacuum

출처 및 근거

ORD 기록
ord-0775f863844649ca90bc5f08c8c246d7
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08389508B2

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