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Dichloromethane → HCID 86700905, 화합물

HRID 625120
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HRID 625120 반응식
[Cl:1][C:2]1[CH:9]=[C:8]([O:10]C)[C:5]([CH:6]=[O:7])=[C:4]([O:12][CH3:13])[CH:3]=1.C(Cl)Cl.B(Br)(Br)Br>>[Cl:1][C:2]1[CH:3]=[C:4]([O:12][CH3:13])[C:5]([CH:6]=[O:7])=[C:8]([OH:10])[CH:9]=1
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참가 물질

4

반응물 3

HCID 6344DichloromethaneHCID 25134Boron tribromideHCID 867009044-Chloro-2,6-dimethoxybenzaldehyde

생성물 1

HCID 86700905HCID 86700905, 화합물수율 99%

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온도
-78 °C

실험 절차

A stirred solution of 4-chloro-2,6-dimethoxybenzaldehyde (Example 37A, 1.95 g, 9.72 mmol) in DCM (20 mL, 311 mmol) at −78° C. was slowly added boron tribromide (9.72 mL, 9.72 mmol). The reaction mixture was stirred at −78° C. for 10 minutes then warmed to r.t. and stirred for 1 hour while monitoring reaction progress by LCMS. Once all s.m. had been consumed, the reaction was quenched with water and extracted with DCM. The organic phase was washed with brine, dried (MgSO4), filtered and concentrated to dryness to give the title material (1.79 g, 9.59 mmol, 99% yield) as a purple solid. LC (Method B): 2.199 min. LCMS (APCI) calcd for C8H8ClO3 [M+H]+ m/z 187.02, found 187.0. 1H NMR (CDCl3, 400 MHz) δ ppm: 11.89 (s, 1H), 10.20 (s, 1H), 6.75 (t, J=2.0 Hz, 1H), 6.66 (m, 1H), 3.91 (s, 1H).

후처리

  1. customat −78° C.
  2. temperaturethen warmed to r.t.
  3. stirringstirred for 1 hour
  4. customreaction progress by LCMS
  5. customhad been consumed
  6. customthe reaction was quenched with water
  7. extractionextracted with DCM
  8. washThe organic phase was washed with brine
  9. dry with materialdried (MgSO4)
  10. filtrationfiltered
  11. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-813a75e4add842199c8a3735eb80a421
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09303065B2

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