Hydrochloric Acid → HCID 67742268, compound

HRID 1707901Notes

Reaction equation

HRID 1707901 reaction equation
[Br:1][C:2]1[CH2:7][C:6]([F:9])(I)[CH:5]=[CH:4][C:3]=1[F:10].[CH2:11]([C:15]1[CH:20]=[CH:19][C:18]([C:21]#[CH:22])=[CH:17][CH:16]=1)[CH2:12][CH2:13][CH3:14].Cl>C(NCC)C.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[Cu]I>[Br:1][C:2]1[C:3]([F:10])=[CH:4][C:5]([C:22]#[C:21][C:18]2[CH:19]=[CH:20][C:15]([CH2:11][CH2:12][CH2:13][CH3:14])=[CH:16][CH:17]=2)=[C:6]([F:9])[CH:7]=1

Participants

7

Reactant 3

HCID 313Hydrochloric AcidHCID 27751321-Butyl-4-ethynylbenzeneHCID 67742270HCID 67742270, compound

Product 1

HCID 67742268HCID 67742268, compoundYield 66.8%

Reagents, catalysts & solvents 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)CatalystHCID 178418476HCID 178418476, compoundCatalystHCID 8021DiethylamineSolvent

Conditions

Temperature
5 °C

Procedure

2-Bromo-1,4-difluoro-4-iodobenzene (11 g) was dissolved in diethylamine (16 ml) under nitrogen atmosphere, and then bis(triphenylphosphine)palladium(II) chloride (0.03 g) and copper(I) iodide (0.03 g) were added thereto, followed by stirring. The flask was cooled to 5° C. or lower, and then 4-butylphenylacetylene (6.2 g) was added dropwise thereto. After stirring at room temperature for 5 hours, the reaction solution was poured into a mixture of concentrated hydrochloric acid (9 ml) and ice (20 g). After extraction with chloroform, the resultant was washed with water twice, followed by distilling off chloroform. The residue was distilled under reduced pressure (b.p. 170° to 180° C./5 mmHg) to give 4-bromo-2,5-difluoro-4'-butyltolane (8 g).

Workup

  1. stirringAfter stirring at room temperature for 5 hours
  2. extractionAfter extraction with chloroform
  3. washthe resultant was washed with water twice
  4. distillationby distilling off chloroform
  5. distillationThe residue was distilled under reduced pressure (b.p. 170° to 180° C./5 mmHg)

Sources & evidence

ORD record
ord-ecd8403da4b24b4ea7dcaf01e1c49f15
Source dataset
uspto-grants-1994_10
Patent number
US05356558

Reaction notes

Loading…