Pyridine → 3-Triphenylmethoxy-1-octyne

HRID 2420401Notes

Reaction equation

HRID 2420401 reaction equation
[CH:1]#[C:2][CH:3]([OH:9])[CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[C:10]1([C:16](Br)([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.N1C=CC=CC=1.[K+].[Br-]>O>[C:10]1([C:16]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[O:9][CH:3]([CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[C:2]#[CH:1])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1

Participants

6

Reactant 4

HCID 1049PyridineHCID 11692BromotriphenylmethaneHCID 131661-Octyn-3-olHCID 253877Potassium Bromide

Product 1

HCID 126753473-Triphenylmethoxy-1-octyne

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

A mixture of 1.26 g (10.0 mmoles) of 1-octyn-3-ol, 4.85 g (15.0 mmoles) of triphenylmethyl bromide, and b 50 ml. of dry pyridine is heated at 95° C. for 60 minutes with occasional swirling. The solution is cooled, treated with water, and extracted with ether. The extract is washed successively with water and saturated sodium chloride solution, dried over magnesium sulfate, and concentrated. The crude product is purified by chromatography on Florisil and recrystallization from petroleum ether to give white crystals, m.p. 65°-66.5°, νmax. (KBr) 3280 (acetylenic hydrogen), 1605, 1030, and 702 cm-1 (triphenylmethoxy group).

Workup

  1. temperatureThe solution is cooled
  2. extractionextracted with ether
  3. washThe extract is washed successively with water and saturated sodium chloride solution
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated
  6. customThe crude product is purified by chromatography on Florisil and recrystallization from petroleum ether
  7. customto give white crystals, m.p. 65°-66.5°, νmax

Sources & evidence

ORD record
ord-de654c2deec64677b74345e44a2ad598
Source dataset
uspto-grants-1978_08
Patent number
US04110368

Reaction notes

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