JP2020503432A5 - - Google Patents
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- Publication number
- JP2020503432A5 JP2020503432A5 JP2019525795A JP2019525795A JP2020503432A5 JP 2020503432 A5 JP2020503432 A5 JP 2020503432A5 JP 2019525795 A JP2019525795 A JP 2019525795A JP 2019525795 A JP2019525795 A JP 2019525795A JP 2020503432 A5 JP2020503432 A5 JP 2020503432A5
- Authority
- JP
- Japan
- Prior art keywords
- radical
- compound
- tert
- radicals
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000034 method Methods 0.000 claims 10
- -1 arylalkyl carbonates Chemical class 0.000 claims 8
- 150000003254 radicals Chemical class 0.000 claims 8
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 6
- 238000006243 chemical reaction Methods 0.000 claims 5
- 150000001875 compounds Chemical class 0.000 claims 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 239000002904 solvent Substances 0.000 claims 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 3
- 150000001491 aromatic compounds Chemical class 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 claims 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims 2
- 150000005840 aryl radicals Chemical class 0.000 claims 2
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 claims 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 claims 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000001624 naphthyl group Chemical group 0.000 claims 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims 1
- CJWNFAKWHDOUKL-UHFFFAOYSA-N 2-(2-phenylpropan-2-yl)phenol Chemical compound C=1C=CC=C(O)C=1C(C)(C)C1=CC=CC=C1 CJWNFAKWHDOUKL-UHFFFAOYSA-N 0.000 claims 1
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 1
- 239000000010 aprotic solvent Substances 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 229910002092 carbon dioxide Inorganic materials 0.000 claims 1
- 239000001569 carbon dioxide Substances 0.000 claims 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 claims 1
- 229910003460 diamond Inorganic materials 0.000 claims 1
- 239000010432 diamond Substances 0.000 claims 1
- 238000003487 electrochemical reaction Methods 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 125000005207 tetraalkylammonium group Chemical group 0.000 claims 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP16198768.0 | 2016-11-15 | ||
| EP16198768.0A EP3321250A1 (de) | 2016-11-15 | 2016-11-15 | Elektrochemisches verfahren zur herstellung von arylalkylcarbonaten und diarylcarbonaten |
| PCT/EP2017/078907 WO2018091370A1 (de) | 2016-11-15 | 2017-11-10 | Elektrochemisches verfahren zur herstellung von arylalkylcarbonaten und diarylcarbonaten |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2020503432A JP2020503432A (ja) | 2020-01-30 |
| JP2020503432A5 true JP2020503432A5 (cg-RX-API-DMAC7.html) | 2020-12-17 |
| JP7037559B2 JP7037559B2 (ja) | 2022-03-16 |
Family
ID=57326227
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019525795A Active JP7037559B2 (ja) | 2016-11-15 | 2017-11-10 | アリールアルキルカーボネートおよびジアリールカーボネートを調製するための電気化学的方法 |
Country Status (7)
| Country | Link |
|---|---|
| EP (2) | EP3321250A1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP7037559B2 (cg-RX-API-DMAC7.html) |
| KR (1) | KR102468537B1 (cg-RX-API-DMAC7.html) |
| CN (1) | CN109937197B (cg-RX-API-DMAC7.html) |
| ES (1) | ES2882510T3 (cg-RX-API-DMAC7.html) |
| TW (1) | TW201831730A (cg-RX-API-DMAC7.html) |
| WO (1) | WO2018091370A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11193212B2 (en) | 2018-09-25 | 2021-12-07 | Sekisui Chemical Co., Ltd. | Synthetic method and synthetic system |
| JP7120098B2 (ja) * | 2019-03-19 | 2022-08-17 | 新東工業株式会社 | テトラヒドロほう酸塩の製造装置、及びテトラヒドロほう酸塩の製造方法 |
| CN115161671B (zh) * | 2022-07-08 | 2025-03-21 | 江西师范大学 | 一种精准区域选择性烯烃芳基化的电化学合成方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3833953A1 (de) | 1988-10-06 | 1990-04-19 | Bayer Ag | Mischungen von speziellen, neuen polycarbonaten mit anderen thermoplasten oder mit elastomeren |
| DE19911746A1 (de) | 1999-03-16 | 2000-09-21 | Basf Ag | Diamantelektroden |
| JP4195717B2 (ja) | 2004-12-24 | 2008-12-10 | 旭化成ケミカルズ株式会社 | 芳香族カーボネートの製造方法 |
| JP2012153909A (ja) * | 2009-08-31 | 2012-08-16 | Tokyo Institute Of Technology | 炭酸ジエステルの製造方法 |
| CN102586799A (zh) * | 2011-01-04 | 2012-07-18 | 索尼公司 | 电解制备碳酸酯的方法 |
| EP2650278A1 (de) | 2012-04-11 | 2013-10-16 | Bayer MaterialScience AG | Verfahren zur Herstellung von Diarylcarbonaten aus Dialkylcarbonaten |
| WO2013186094A2 (en) * | 2012-06-15 | 2013-12-19 | Basf Se | Anodic oxidation of organic substrates in the presence of nucleophiles |
-
2016
- 2016-11-15 EP EP16198768.0A patent/EP3321250A1/de not_active Ceased
-
2017
- 2017-11-10 KR KR1020197013452A patent/KR102468537B1/ko active Active
- 2017-11-10 WO PCT/EP2017/078907 patent/WO2018091370A1/de not_active Ceased
- 2017-11-10 JP JP2019525795A patent/JP7037559B2/ja active Active
- 2017-11-10 CN CN201780070941.4A patent/CN109937197B/zh active Active
- 2017-11-10 EP EP17801651.5A patent/EP3541778B1/de active Active
- 2017-11-10 ES ES17801651T patent/ES2882510T3/es active Active
- 2017-11-13 TW TW106139094A patent/TW201831730A/zh unknown
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