Acetone → HCID 10878747, compound

HRID 1955352Notes

Reaction equation

HRID 1955352 reaction equation
[CH2:1]([OH:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+].[H][H].Cl[CH2:14][C@H:15]([OH:18])[CH2:16][OH:17].Cl.[CH3:20][C:21]([CH3:23])=O>C1(C)C=CC(S(O)(=O)=O)=CC=1.C(N(CC)CC)C.CN(C=O)C>[CH2:1]([O:8][CH2:14][C@H:15]1[CH2:16][O:17][C:21]([CH3:23])([CH3:20])[O:18]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

10

Reactant 6

HCID 180AcetoneHCID 244Benzyl AlcoholHCID 313Hydrochloric AcidHCID 24758Sodium hydrideHCID 148793(2R)-3-Chloro-1,2-propanediolHCID 178418361HCID 178418361, compound

Product 1

HCID 10878747HCID 10878747, compoundYield 54%

Reagents, catalysts & solvents 3

HCID 6101p-Toluenesulfonic acidCatalystHCID 6228DimethylformamideSolvent2×HCID 8471TriethylamineSolvent

Conditions

Temperature
60 °C

Procedure

Benzyl alcohol (32.90 g, 0.35 mol) was dropped under ice cooling in a suspension of 60% sodium hydride (5.88 g, 0.155 mol) and DMF (150 ml) After emission of hydrogen gas, therein a DMF solution (15 ml) of (R)-3-chloro-1,2-propanediol (8.535 g, 0.078 mol, optical purity 98.7% e.e.) was dropped. The reaction temperature was raised to 60° C. and the mixture was stirred under heating for 2 hours. After completion of the reaction the mixture was cooled on ice bath and neutralized with 6% hydrochloric acid. After removal of water and DMF in vacuo, ethyl acetate was added to the residue, the insoluble materials were filtered off and the filtrate was condensed in vacuo. Thereto acetone (750 ml) and p-toluenesulfonic acid (0.579 g), were added and the solution was stirred for 5 hours at 25° C. After the reaction was over, the mixture was neutralized with triethylamine. After stirring for 5 minutes, acetone was removed in vacuo. The crude product was distilled to give 9.267 g of (S)-4-benzyloxymethyl-2,2-dimethyl-1,3-dioxolane (yield 54%, b.p. 110° C. at 0.3 mmHg).

Workup

  1. temperatureunder heating for 2 hours
  2. customAfter completion of the reaction the mixture
  3. temperaturewas cooled on ice bath
  4. customAfter removal of water and DMF in vacuo, ethyl acetate
  5. additionwas added to the residue
  6. filtrationthe insoluble materials were filtered off
  7. customcondensed in vacuo
  8. stirringthe solution was stirred for 5 hours at 25° C
  9. stirringAfter stirring for 5 minutes
  10. customacetone was removed in vacuo
  11. distillationThe crude product was distilled

Sources & evidence

ORD record
ord-ac3cacdb4c344828883bcd01d3e04b21
Source dataset
uspto-grants-2000_09
Patent number
US06124479

Reaction notes

Loading…