Dimethylformamide → HCID 21919639, compound

HRID 507706Notes

Reaction equation

HRID 507706 reaction equation
CN([CH:4]=[O:5])C.[C:6](Cl)(=[O:10])[C:7](Cl)=O.[CH2:12]([O:14][C:15]#[CH:16])[CH3:13].C(N([CH2:22][CH3:23])CC)C.[CH2:24](Cl)Cl>>[CH2:15]([O:14][C:12]1[C:24]2([CH2:7][CH2:6][O:10][CH2:23][CH2:22]2)[C:4](=[O:5])[CH:13]=1)[CH3:16]

Participants

6

Reactant 5

HCID 6228DimethylformamideHCID 6344DichloromethaneHCID 8471TriethylamineHCID 61239Ether, ethyl ethynylHCID 65578Oxalyl chloride

Product 1

HCID 21919639HCID 21919639, compoundYield 59%

Procedure

Tetrahydropyranyl-4-carboxylic acid (14.7 g, 0.11 mol) and DMF (0.5 ml) in DCM (150 ml) was treated dropwise with oxalyl chloride (1.1 eq, 10.9 ml, 0.12 mol). After 1 h the reaction mixture was concentrated in vacuo and the residual slurry was diluted with Et2O (200 ml) and the resulting precipitate removed by filtration. The filtrate was treated with ethoxyacetylene (40% w/w solution in hexanes, 1.3 eq, 18 ml) followed dropwise with triethylamine (25 ml, 0.19 mol) and the reaction stirred for lid. Filtration and concentration of the filtrate in vacuo followed by chromatography (SiO2, 5:1 EtOAc:hexanes) gave the title compound as a pale yellow oil (12.1 g, 59%). δH (CDCl3, 300K) 4.85 (1H, s), 4.23 (2H, q, J 7.1 Hz), 3.89-3.75 (4H, m), 1.88-1.79 (4H, m), 1.47 (3H, t, J 7.1 Hz); m/z (ES+, 70V) 182.9 (MH+).

Workup

  1. concentrationAfter 1 h the reaction mixture was concentrated in vacuo
  2. additionthe residual slurry was diluted with Et2O (200 ml)
  3. customthe resulting precipitate removed by filtration
  4. filtrationFiltration and concentration of the filtrate in vacuo

Sources & evidence

ORD record
ord-3d3b1c7ddc8640cbbb7bda7d897ead50
Source dataset
uspto-grants-2010_08
Patent number
US07786177B2

Reaction notes

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