Water → Boma

HRID 7733

반응식

HRID 7733 반응식
Br[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[O:10][C:11]3[CH:17]=[CH:16][CH:15]=[CH:14][C:12]=3[N:13]=2)=[CH:5][C:4]=1[O:18][CH3:19].O.[C-:21]#[N:22].[Na+]>CN(C)C=O>[O:10]1[C:11]2[CH:17]=[CH:16][CH:15]=[CH:14][C:12]=2[N:13]=[C:9]1[C:6]1[CH:7]=[CH:8][C:3]([CH2:2][C:21]#[N:22])=[C:4]([O:18][CH3:19])[CH:5]=1

참가 물질

5

반응물 3

HCID 962WaterHCID 8929Sodium CyanideHCID 219909912-[4-(Bromomethyl)-3-methoxyphenyl]-1,3-benzoxazole

생성물 1

HCID 10192854Boma

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

A mixture of, 2-[4-(bromomethyl)-3-methoxyphenyl]-1,3-benzoxazole (318 mg, 1 mmol), dimethylformamide (7.5 mL) and deionzed water (2.5 mL) was stirred at rt. Sodium cyanide (150 mg, 3.0 mmol) was added to reaction. After 3 h, dimethylformamide (10 mL) was added to help dissolve solids in reaction mixture. Let reaction mixture stir overnight at rt. Workup was done by washing reaction with brine (3×30 mL), extraction with EtOAc, combined organic extracts, dried (Na2SO4), filtered and removed solvent in vacuo. Flash chromatography of resulting orange solid on silica gel using a gradient elution of 1:9 EtOAc:hexanes to 1:3 EtOAc:hexanes afforded the desired intermediate, [4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]acetonitrile, as a light yellow solid.

후처리

  1. dissolutionto help dissolve solids
  2. customin reaction mixture
  3. customreaction mixture
  4. stirringstir overnight at rt
  5. washby washing
  6. customreaction
  7. extractionwith brine (3×30 mL), extraction with EtOAc
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. customremoved solvent in vacuo
  11. customFlash chromatography of resulting orange solid on silica gel using
  12. washa gradient elution of 1:9 EtOAc

출처 및 근거

ORD 기록
ord-4d49f2de2fea4e568118fe4805b7b8f7
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07087601B2

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