2-Butyn-1-ol → HCID 18353850, compound

HRID 430035Notes

Reaction equation

HRID 430035 reaction equation
[Cl-].[Ca+2].[Cl-].Br[CH2:5][C:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=[CH:8][CH:7]=1.[CH2:16]([OH:20])[C:17]#[C:18][CH3:19]>[O-2].[Zn+2].ClC(Cl)C>[CH2:16]([O:20][CH2:5][C:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=[CH:8][CH:7]=1)[C:17]#[C:18][CH3:19]

Participants

6

Reactant 3

HCID 129912-Butyn-1-olHCID 1378441-(Bromomethyl)naphthaleneHCID 5284359Calcium Chloride

Product 1

HCID 18353850HCID 18353850, compound

Reagents, catalysts & solvents 2

HCID 3007857Zinc OxideCatalystHCID 63651,1-DichloroethaneSolvent

Procedure

To a flask equipped with magnetic stirrer, condenser and drying tube filled with calcium chloride, bromomethylnaphthalene (1.0 g, 4.52 mmol), 2-butyn-1-ol (0.63 g, 9 mmol) and 10 ml of dichloroethane are placed. After the addition of zinc(II) oxide (4.0 g, 4.52 mmol) the suspension is stirred for 1 hour at room temperature, then it is refluxed for 1 hour. The reaction is accompanied by a characteristic change of colour. The mixture is then filtered, the filtrate is evaporated. The residual oil is dissolved in 15 ml of ether, washed with 2×50 ml of water, dried and evaporated. The product is purified by coloumn chromatography. Purity (GC) 95%. IR (CHCl3, cm−1) υ: 3044, 3001, 2945, 2920, 2854, 1598, 1509, 1356, 1166, 1086, 1067; 1H-NMR (400 MHz, CDCl3) δ: 1.93 (3H, t, J=2.3 Hz, C≡C—CH3), 4.22 (2H, q, J=2.1 Hz, O—CH2—C≡C), 5.06 (2H, s, C10H7—CH2—O), 7.45 (1H, t, J=8 Hz), 7.53 (3H, m), 7.84 (1H, d, J=8.1 Hz), 7.88 (3H, m), 7.88 (1H, d, J=7.7 Hz), 8.19 (1H, d, J=8.2 Hz); 13C-NMR (100 MHz, CDCl3) δ: 3.6 (C≡C—CH3), 57.71 (O—CH2—C≡C), 69.72 C10H7—CH2—O), 75.10 (O—CH2—C≡C), 82.76 (O—CH2—C≡C), 124.03, 125.10, 125.72, 126.19, 126.85, 128.43, 128.72, 131.79 (C-8a), 133.06, 133.70.

Workup

  1. customTo a flask equipped with magnetic stirrer, condenser
  2. customdrying tube
  3. temperatureit is refluxed for 1 hour
  4. filtrationThe mixture is then filtered
  5. customthe filtrate is evaporated
  6. dissolutionThe residual oil is dissolved in 15 ml of ether
  7. washwashed with 2×50 ml of water
  8. customdried
  9. customevaporated
  10. customThe product is purified by coloumn chromatography

Sources & evidence

ORD record
ord-116c9ef315dd4b4ea46a3f3d637df659
Source dataset
uspto-grants-2001_11
Patent number
US06320085B1

Reaction notes

Loading…