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Tetrahydrofuran → 5-(Hydroxymethyl)-2-methoxybenzonitrile

HRID 1370117
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HRID 1370117 반응식
[C:1]([C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][C:12]=1[O:13][CH3:14])[C:6](OC)=[O:7])#[N:2].O1CCCC1.[BH4-].[Na+].[Cl-].[NH4+]>CO>[C:1]([C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][C:12]=1[O:13][CH3:14])[CH2:6][OH:7])#[N:2]
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참가 물질

6

반응물 4

HCID 8028TetrahydrofuranHCID 25517Ammonium ChlorideHCID 2801011Methyl 3-cyano-4-methoxybenzoateHCID 4311764Sodium borohydride

생성물 1

HCID 229961945-(Hydroxymethyl)-2-methoxybenzonitrile

시약·촉매·용매 1

HCID 887Methanol용매

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온도
45 °C

실험 절차

A mixture of methyl 3-cyano-4-methoxybenzoate (5g), tetrahydrofuran (25 mL) and sodium borohydride (1.98 g) was heated at 45° C. The mixture was dropwise added with methanol (6.36 mL) at 45-55° C. over 15 minutes and then refluxed for 3.5 hours. After cooling to 0° C., the mixture was added with an aqueous saturated ammonium chloride solution at the same temperature. The mixture was stirred at room temperature for an hour, and extracted with ethyl acetate. The organic layer was washed successively with water, an aqueous saturated sodium bicarbonate solution and brine. The organic layer was dried over magnesium sulfate and evaporated in vacuo. The residual solid was triturated with diisopropyl ether to give 3-cyano-4-methoxybenzyl alcohol (3.75 g) as a pale brown solid.

후처리

  1. temperaturerefluxed for 3.5 hours
  2. temperatureAfter cooling to 0° C.
  3. extractionextracted with ethyl acetate
  4. washThe organic layer was washed successively with water
  5. dry with materialThe organic layer was dried over magnesium sulfate
  6. customevaporated in vacuo
  7. customThe residual solid was triturated with diisopropyl ether

출처 및 근거

ORD 기록
ord-2eac81fda89446a4b3e3943bce64e0c8
출처 데이터셋
uspto-grants-2003_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06582351B1

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