Boron trifluoride etherate → HCID 13290025, compound

HRID 485869Notes

Reaction equation

HRID 485869 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[CH:9](OCO)[CH:8]([CH:13]3[CH2:17][CH2:16][CH2:15][CH2:14]3)[S:7][C:6]=2[C:18]=1[Cl:19].B(F)(F)F.C[CH2:25][O:26]CC.[OH-].[Na+]>C(O)(=O)C>[Cl:1][C:2]1[C:3]([O:26][CH3:25])=[CH:4][C:5]2[CH:9]=[C:8]([CH:13]3[CH2:14][CH2:15][CH2:16][CH2:17]3)[S:7][C:6]=2[C:18]=1[Cl:19]

Participants

5

Procedure

A mixture of 2.5 g of 6,7-dichloro-2-cyclopentyl-2,3-dihydro-3-hydroxymethoxybenzo[b]thiophene and 10 ml of glacial acetic acid containing 5 ml of boron trifluoride etherate is warmed on a steam bath for 15 minutes and allowed to stand overnight. The mixture is poured into a chilled solution of dilute sodium hydroxide and the organic material is extracted into ether. Washing with water, followed by drying over anhydrous magnesium sulfate and evaporation in vacuo, gives 2.0 g of wax-like crystals. Recrystallization from ether-hexane gives 1.8 g of 6,7-dichloro-2-cyclopentyl-5-methoxybenzo-[b]thiophene as fine needles, mp 59.5°-60°.

Workup

  1. temperatureis warmed on a steam bath for 15 minutes
  2. extractionthe organic material is extracted into ether
  3. washWashing with water
  4. dry with materialby drying over anhydrous magnesium sulfate and evaporation in vacuo
  5. customgives 2.0 g of wax-like crystals
  6. customRecrystallization from ether-hexane

Sources & evidence

ORD record
ord-ba90fd4040f54d64aa574e311bbeb491
Source dataset
uspto-grants-1985_08
Patent number
US04537976

Reaction notes

Loading…