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Tetrabutylammonium Fluoride → 3-Hydroxymethyl-5-methoxymethyl-benzonitrile

HRID 1167338
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반응식

HRID 1167338 반응식
C([SiH2][O:6][C:7](C)(C)[C:8]1[CH:9]=[C:10]([CH:13]=[C:14]([CH2:16][O:17][CH3:18])[CH:15]=1)[C:11]#[N:12])(C)(C)C.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1>[OH:6][CH2:7][C:8]1[CH:9]=[C:10]([CH:13]=[C:14]([CH2:16][O:17][CH3:18])[CH:15]=1)[C:11]#[N:12]
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참가 물질

4

반응물 2

HCID 2724141Tetrabutylammonium FluorideHCID 1373287443-(Tert-butyl-dimethyl-silanyloxymethyl)-5-methoxymethyl-benzonitrile

생성물 1

HCID 229962313-Hydroxymethyl-5-methoxymethyl-benzonitrile수율 84%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 3-(tert-butyl-dimethyl-silanyloxymethyl)-5-methoxymethyl-benzonitrile (1.402 g, 4.810 mmol) in tetrahydrofuran (10 mL) at room temperature was added tetrabutylammonium fluoride (5.051 mL, 5.051 mmol, 1 M in tetrahydrofuran). The reaction mixture was stirred at room temperature for 2 h then concentrated in vacuo. Purification of the residue by flash chromatography (Biotage system, KP-Sil™ 32-63 μm, 60 Å silica gel) eluting with 40% ethyl acetate in hexanes yielded 3-hydroxymethyl-5-methoxymethyl-benzonitrile (713 mg, 84%).

후처리

  1. concentrationthen concentrated in vacuo
  2. customPurification of the residue by flash chromatography (Biotage system, KP-Sil™ 32-63 μm, 60 Å silica gel)
  3. washeluting with 40% ethyl acetate in hexanes

출처 및 근거

ORD 기록
ord-eb81b3a6fd434475a1a59db0f2e30ac0
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06617346B1

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