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Diphenylmethane diisocyanate → Urea Urethane

HRID 561260
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HRID 561260 반응식
C(O)C[CH2:3][CH2:4][OH:5].C([O-])(=O)CCCCCCCCCCC.C([O-])(=O)CCCCCCCCCCC.C([Sn+2]CCCC)CCC.C1C(CC2C=CC([N:57]=[C:58]=[O:59])=CC=2)=CC=C([N:60]=[C:61]=[O:62])C=1.CCCCO[C@H](CO)CC.C[N:74]1CCCC1=O>C(OCC)C.CO>[NH2:57][C:58]([O:5][CH2:4][CH3:3])=[O:59].[NH2:74][C:61]([NH2:60])=[O:62]
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참가 물질

8

반응물 5

HCID 7570Diphenylmethane diisocyanateHCID 80641,4-ButanediolHCID 13387N-methyl-2-pyrrolidone4회HCID 3084433CID 3084433HCID 9809426Di-n-butyldilauryltin

생성물 1

HCID 21585015Urea Urethane수율 77.2%

시약·촉매·용매 2

HCID 887Methanol용매
HCID 3283Diethyl Ether용매

실험 절차

In an argon atmosphere, 1,4-butanediol (0.240 g, 2.66 mmol) and dibutyltin dilaurate (0.2 ml) were dissolved in N-methylpyrrolidinone (7.00 ml) in a three-necked flask. A solution of 4,4′-diphenylmethane diisocyanate (2.00 g, 7.99 mmol) in N-methylpyrrolidinone (7.00 ml) was slowly added dropwise to the solution at room temperature. After the completion of the dropwise addition, the solution was reacted at 50° C. for 2 hours. Thereafter, a solution of the compound (6) from Example 1 (1.69 g, 2.66 mmol) in N-methylpyrrolidinone (3.00 ml) was slowly added dropwise to the reaction solution at 0° C., followed by reaction at 0° C. for 0.5 hour. After the completion of the reaction, a solution of polytetramethylene glycol (2.66 g, 2.66 mmol) in N-methylpyrrolidinone (3.00 ml) was slowly added dropwise to the reaction solution at 0° C., followed by reaction at 50° C. overnight. The resultant reaction solution was poured into an excess of a solvent mixture (methanol:diethyl ether=1:1 (by volume)). The precipitate caused was suction filtered and dried under reduced pressure to give a segmented poly(urethane-urea) with a phosphorylcholine group represented by Formula SPUU-2 above as a brown solid (weight: 5.09 g, yield: 77.2%). The structure of the polymer was determined from the IR spectrum given below. From the 1H-NMR spectrum, the phosphorylcholine group content in the polymer SPUU-2 was found to be 19.7 mol %.

후처리

  1. additionAfter the completion of the dropwise addition
  2. customthe solution was reacted at 50° C. for 2 hours
  3. customfollowed by reaction at 0° C. for 0.5 hour
  4. customAfter the completion of the reaction
  5. customfollowed by reaction at 50° C. overnight
  6. customThe resultant reaction solution
  7. filtrationfiltered
  8. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-63e90ffa79f94b35947b9f9175e32ac3
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08063238B2

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