3-Bromothiophene → 1-butyl-alpha-(3-thienyl)-1H-benzotriazole-5-methanol

HRID 2166040Notes

Reaction equation

HRID 2166040 reaction equation
Br[C:2]1[CH:6]=[CH:5][S:4][CH:3]=1.C([Li])CCC.[CH2:12]([N:16]1[C:20]2[CH:21]=[CH:22][C:23]([CH:25]=[O:26])=[CH:24][C:19]=2[N:18]=[N:17]1)[CH2:13][CH2:14][CH3:15]>CCCCCC.O(CC)CC>[CH2:12]([N:16]1[C:20]2[CH:21]=[CH:22][C:23]([CH:25]([C:2]3[CH:6]=[CH:5][S:4][CH:3]=3)[OH:26])=[CH:24][C:19]=2[N:18]=[N:17]1)[CH2:13][CH2:14][CH3:15]

Participants

6

Reactant 3

HCID 133833-BromothiopheneHCID 14990615butyl-1H-benzotriazole-5-carboxaldehydeHCID 178418339Butyllithium

Product 1

HCID 149906161-butyl-alpha-(3-thienyl)-1H-benzotriazole-5-methanolYield 58.9%

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolvent2×HCID 8058HexaneSolvent

Procedure

To a stirred and cooled (-78° C.) solution of 7.2 parts of 3-bromothiophene in 70 parts of 1,1'-oxybisethane were added 30 parts of a 1-butyllithium solution 1.6M in hexane. After stirring for 20 minutes at this low temperature, a solution of 6 parts of 1-butyl-1H-benzotriazole-5-carboxaldehyde in 1,1'-oxybisethane was added to the previous mixture. The reaction mixture was stirred for 2 hours at -78°~-'° C. The whole was poured into 200 parts of ice water and the product was extracted three times with 56 parts of 1,1'-oxybisethane. The combined extracts were dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of dichloromethane and methanol (98:2 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2,2'-oxybispropane. The product was filtered off and dried, yielding 5 parts (58.9%) of 1-butyl-α-(3-thienyl)-1H-benzotriazole-5-methanol; mp. 80° C. (int. 58).

Workup

  1. stirringAfter stirring for 20 minutes at this low temperature
  2. stirringThe reaction mixture was stirred for 2 hours at -78°~-'° C
  3. extractionthe product was extracted three times with 56 parts of 1,1'-oxybisethane
  4. customThe combined extracts were dried
  5. filtrationfiltered
  6. customevaporated
  7. customThe residue was purified by column chromatography over silica gel using
  8. additiona mixture of dichloromethane and methanol (98:2 by volume) as eluent
  9. customThe pure fractions were collected
  10. customthe eluent was evaporated
  11. customThe residue was crystallized from 2,2'-oxybispropane
  12. filtrationThe product was filtered off
  13. customdried

Sources & evidence

ORD record
ord-e1f17b5424a34446b5cdff468b9d9c8a
Source dataset
uspto-grants-1990_07
Patent number
US04943574

Reaction notes

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