Carbon Dioxide → HCID 14478664, compound

HRID 1905077Notes

Reaction equation

HRID 1905077 reaction equation
[CH2:1]([C:3]1([O:7][CH2:6]1)[CH2:4][OH:5])[CH3:2].[C:8](=O)=O.[CH:11]([Mg]Br)=[CH2:12].Cl>O1CCCC1.[Cu](I)I.C(#N)C>[CH2:1]([C:3]([OH:7])([CH2:6][CH2:8][CH:11]=[CH2:12])[CH2:4][OH:5])[CH3:2]

Participants

8

Conditions

Temperature
-27.5 °C

Procedure

A mixture of 2 R 2-ethyl-2,3-epoxypropanol (2.6 g, 25.5 mmol) and copper iodide (475 mg, 2.5 mmol) was stirred in tetrahydrofuran (50 mL) under nitrogen and brought to -30° C. (dry ice, acetonitrile). Vinyl magnesium bromide [32 mL, 2 M in tetrahydrofuran (THF), 2.5 eq] was added from a dropping funnel at such a rate as to maintain the temperature at -25 to -30° C. The reaction mixture was stirred at -30° C. for 2 h then brought to 0° C. and acidified with 10% HCl. The THF layer was separated and the aqueous phase was extracted with ether (3×50 mL). The organic layers were combined, dried over sodium sulfate, oncentrated and distilled to give the title compound as a clear colorless oil (2.2 g, 60%, b.p. 85° C./5 mm). TLC Rf 0.26 (silica gel, 5% MeOH in CH2Cl2, CAS/char:brown).

Workup

  1. custombrought to -30° C.
  2. customthen brought to 0° C.
  3. customThe THF layer was separated
  4. extractionthe aqueous phase was extracted with ether (3×50 mL)
  5. dry with materialdried over sodium sulfate
  6. distillationdistilled

Sources & evidence

ORD record
ord-0a6e5c0b301b45e8b69d6bf317bcd436
Source dataset
uspto-grants-1989_06
Patent number
US04841045

Reaction notes

Loading…