Water → HCID 22601992, compound

HRID 2308388Notes

Reaction equation

HRID 2308388 reaction equation
C(N(CC)CC)C.Cl[CH2:9][CH2:10][C:11]([S:13][CH2:14][CH:15]1[S:19][CH:18]([CH2:20][O:21][C:22](=[O:26])[CH2:23][CH2:24]Cl)[CH2:17][S:16]1)=[O:12].O.C1(C)C=CC=CC=1>CC(C)=O>[C:11]([S:13][CH2:14][CH:15]1[S:19][CH:18]([CH2:20][O:21][C:22](=[O:26])[CH:23]=[CH2:24])[CH2:17][S:16]1)(=[O:12])[CH:10]=[CH2:9]

Participants

6

Reactant 4

HCID 962WaterHCID 1140TolueneHCID 8471TriethylamineHCID 22602212HCID 22602212, compound

Product 1

HCID 22601992HCID 22601992, compoundYield 77%

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

Next, 40.0 g (0.39 mol) of triethylamine was added dropwise to a solution of 50.0 g (0.13 mol) of 2-(3-chloropropionylthiomethyl)-4-(3-chloropropionyloxymethyl)-1,3-dithiolan prepared above dissolved in 195 g of acetone at 2 to 5° C. in 1 hour. They were allowed to react at the same temperature for 1.5 hours, with stirring, to which 520 g of water was added. The resultant mixture was treated with 520 g of toluene to extract the reaction product. The extract organic phase (toluene solution) was washed with water until the aqueous phase turned neutral. Then, the organic phase was separated out, incorporated with 0.12 g of 4-methoxyphenol as a polymerization inhibitor, and distilled under a vacuum to be concentrated while removing toluene, to obtain a lightly yellowish, transparent liquid as a crude product. The crude product thus prepared was purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate mixture), to obtain 29.0 g of 2-acryloylthiomethyl-4-acryloyloxymethyl-1,3-dithiolan, which was a colorless, transparent liquid, in a yield of 77%.

Workup

  1. customprepared
  2. customto react at the same temperature for 1.5 hours
  3. additionwas added
  4. extractionto extract the reaction product
  5. washThe extract organic phase (toluene solution) was washed with water until the aqueous phase
  6. customThen, the organic phase was separated out, incorporated with 0.12 g of 4-methoxyphenol as a polymerization inhibitor
  7. distillationdistilled under a vacuum
  8. concentrationto be concentrated
  9. customwhile removing toluene
  10. customto obtain a lightly yellowish, transparent liquid as a crude product
  11. customwas purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate mixture)

Sources & evidence

ORD record
ord-2b43d025aa8448c781e606e6546f4b07
Source dataset
uspto-grants-2004_12
Patent number
US06835844B2

Reaction notes

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