Dichloromethane → HCID 178515546, compound

HRID 1391356Notes

Reaction equation

HRID 1391356 reaction equation
O[C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:11]2C=CC(O)=CC=2)(C)C)=[CH:4][CH:3]=1.C(Cl)Cl.[C:21](Cl)(Cl)=[O:22].C([N:27](CC)CC)C>[OH-].[Na+]>[OH:22][C:21]1[CH:11]=[CH:8][C:5]2[C:4](=[CH:3][CH:2]=[CH:7][CH:6]=2)[N:27]=1

Participants

6

Reactant 4

HCID 6344DichloromethaneHCID 6371PhosgeneHCID 6623Bisphenol AHCID 8471Triethylamine

Product 1

HCID 178515546HCID 178515546, compound

Reagents, catalysts & solvents 1

HCID 14798Sodium HydroxideSolvent2×

Procedure

456 g of bisphenol A and 559 g of 2-[4-hydroxyphenyl]-2-[5-(8-hydroxyquinolyl)]-propane are dissolved in 4 kg of 9% strength sodium hydroxide solution and 9 kg of methylene chloride are then added. 562.8 g of phosgene are introduced with vigorous stirring and 60 ml of a 4% strength triethylamine solution are then added dropwise. The mixture is stirred for a further hour and if necessary sufficient sodium hydroxide solution is added for the pH of the solution to remain constant at 13. The phases are separated and the aqueous phase is tested for complete conversion. The organic phase is extracted once with 5% strength H3PO4, washed with water until neutral and subsequently dried over sodium-sulphate. The organic phase is concentrated and the short-chain polycarbonate with hydroxyquinoline end groups is obtained direct by precipitation in methanol.

Workup

  1. additionare then added
  2. additionis added for the pH of the solution
  3. customThe phases are separated
  4. extractionThe organic phase is extracted once with 5% strength H3PO4
  5. washwashed with water until neutral and
  6. dry with materialsubsequently dried over sodium-sulphate
  7. concentrationThe organic phase is concentrated

Sources & evidence

ORD record
ord-6b3eca97bb464c1abbb86602996747c7
Source dataset
uspto-grants-1979_02
Patent number
US04142035

Reaction notes

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