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Sodium borohydride → HCID 69353261, 화합물

HRID 1349940
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HRID 1349940 반응식
[BH4-].[Na+].[Br:3][C:4]1[CH:5]=[C:6]([N+:14]([O-:16])=[O:15])[C:7]([O:12][CH3:13])=[C:8]([CH:11]=1)[CH:9]=[O:10]>CO.O1CCCC1>[Br:3][C:4]1[CH:5]=[C:6]([N+:14]([O-:16])=[O:15])[C:7]([O:12][CH3:13])=[C:8]([CH:11]=1)[CH2:9][OH:10]
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참가 물질

5

반응물 2

HCID 4311764Sodium borohydrideHCID 210937475-Bromo-2-methoxy-3-nitrobenzaldehyde

생성물 1

HCID 69353261HCID 69353261, 화합물수율 82.3%

시약·촉매·용매 2

HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

Sodium borohydride (4 g) was added in portions to a stirring solution of crude 5-bromo-2-methoxy-3-nitrobenzaldehyde (20.5 g) in methanol (350 mL) and tetrahydrofuran (150 mL) at 0° C. After 1 h, the methanol was removed in vacuo. The residue was treated with cold water (150 mL) and extracted with diethyl ether (2×150 mL). The combined organic layer was evaporated in vacuo to give a crude oil. Silica gel chromatography eluting with ethyl acetate in petroleum ether (10–40%) gave the title compound (17 g) as a solid.

후처리

  1. customthe methanol was removed in vacuo
  2. additionThe residue was treated with cold water (150 mL)
  3. extractionextracted with diethyl ether (2×150 mL)
  4. customThe combined organic layer was evaporated in vacuo
  5. customto give a crude oil
  6. washSilica gel chromatography eluting with ethyl acetate in petroleum ether (10–40%)

출처 및 근거

ORD 기록
ord-1f72f1a800ac48aeb6e9e41e2e9b490f
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07214674B2

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