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Diphenyl carbonate → Methyl 4-methylbenzoate

HRID 861678
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HRID 861678 반응식
[C:1]1([CH3:16])[CH:6]=[CH:5][C:4]([C:7]([O:9][C:10]2C=CC=CC=2)=[O:8])=[CH:3][CH:2]=1.C(=O)(OC)OC.C(=O)(OC1C=CC=CC=1)OC.C(=O)(OC1C=CC=CC=1)OC1C=CC=CC=1>CC(C)[O-].CC(C)[O-].CC(C)[O-].CC(C)[O-].[Ti+4]>[C:1]1([CH3:16])[CH:2]=[CH:3][C:4]([C:7]([O:9][CH3:10])=[O:8])=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 7597Diphenyl carbonateHCID 12021Dimethyl CarbonateHCID 139482Carbonic acid, methyl phenyl esterHCID 219444Phenyl 4-methylbenzoate

생성물 1

HCID 7455Methyl 4-methylbenzoate수율 33%

시약·촉매·용매 1

HCID 11026Titanium isopropoxide
촉매

실험 절차

Into an autoclave made of SUS316 having an internal volume of 100 ml were charged the synthesized phenyl p-toluate 30 g (141 mmole), dimethyl carbonate 6.37 g (70.7 mmole) and titanium tetraisopropoxide 0.80 g (2.83 mmole). The pressure was elevated to 20 kg/cm2 with nitrogen, and the contents were then reacted for three hours at 180° C. After completing the reaction, the reaction mixture was analyzed by gas chromatography. As a result, the yield of methyl phenyl carbonate was 18%, and the yield of diphenyl carbonate was 15%. Furthermore, at the same time, methyl p-toluate was produced as a by-product with a yield of 33% (the yield is given in terms of phenyl p-toluate).

후처리

  1. customthe contents were then reacted for three hours at 180° C
  2. customthe reaction

출처 및 근거

ORD 기록
ord-1be5ddf35f2f412190bebfbab557a239
출처 데이터셋
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05714627

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