Hydrochloric Acid → HCID 5948860, compound

HRID 358245Notes

Reaction equation

HRID 358245 reaction equation
[Li].[CH:2](/Cl)=[CH:3]\[CH3:4].C(/[Li])=C\C.[C:10]1([C:16](=[O:21])[C:17]([O:19][CH3:20])=[O:18])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.Cl>CCCCCC.CCOCC>[C:10]1([C:16](/[CH:2]=[CH:3]/[CH3:4])([OH:21])[C:17]([O:19][CH3:20])=[O:18])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1

Participants

8

Reactant 5

HCID 313Hydrochloric AcidHCID 84835Methyl phenylglyoxalateHCID 3028194LithiumHCID 5284364trans-1-ChloropropeneHCID 178506894HCID 178506894, compound

Product 1

HCID 5948860HCID 5948860, compound

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolvent2×HCID 8058HexaneSolvent

Procedure

Lithium ribbon (1.0% Na content) 6.9 g., 1.0 g. at.) was cut into strips (1.0 cm.=0.089 g.), degreased in hexane and cut into thin strips into ether (200 ml.) under helium. The reaction flask was equipped with dry-ice condenser and trans-propenyl chloride (25.5 g., 0.30 mole) was introduced dropwise during 60 minutes to the rapidly stirred suspension. The reaction was exothermic and was controlled by the addition of the halide. After addition the mixture was stirred for an additional 60 minutes. The trans-propenyllithium slurry was subsequently siphoned (in spurts during 30 minutes by He.pressure) into a stirred solution containing methyl phenylglyoxylate (55.0 g., 0.3 mole) in ether which was cooled to -78°. After 30 minutes of additional stirring, the reaction was warmed to -10° and poured onto 30 ml. of concentrated HCl and ca. 200 g. of ice. The ether layer was separated and the aqueous layer was further extracted with 3×50 ml. of ether. All ether layers were combined and dried over Drierite for 18 hours. After the solvent was stripped, the crude product weighting 58.1 g. (94%) was obtained which on distillation afforded 35 g. (57%) of pure material, b.p. 100° (0.05 mm.).

Workup

  1. customThe reaction flask was equipped with dry-ice condenser
  2. additionAfter addition the mixture
  3. custom(in spurts during 30 minutes by He.pressure)
  4. temperaturewas cooled to -78°
  5. waitAfter 30 minutes of additional stirring
  6. temperaturethe reaction was warmed to -10°
  7. additionpoured onto 30 ml
  8. customThe ether layer was separated
  9. extractionthe aqueous layer was further extracted with 3×50 ml
  10. dry with materialdried over Drierite for 18 hours
  11. custom(94%) was obtained which
  12. distillationon distillation
  13. customafforded 35 g

Sources & evidence

ORD record
ord-0ab58b02b8814c70a42d0ce0a1f90b67
Source dataset
uspto-grants-1984_08
Patent number
US04465834

Reaction notes

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