KR840002770A - 아세토페논유도체의 제조방법 - Google Patents
아세토페논유도체의 제조방법 Download PDFInfo
- Publication number
- KR840002770A KR840002770A KR1019820005547A KR820005547A KR840002770A KR 840002770 A KR840002770 A KR 840002770A KR 1019820005547 A KR1019820005547 A KR 1019820005547A KR 820005547 A KR820005547 A KR 820005547A KR 840002770 A KR840002770 A KR 840002770A
- Authority
- KR
- South Korea
- Prior art keywords
- organic solvent
- hydrophilic organic
- alkali metal
- compound
- acid acceptor
- Prior art date
Links
- 150000008062 acetophenones Chemical class 0.000 title claims 2
- 238000004519 manufacturing process Methods 0.000 title claims 2
- 239000002253 acid Substances 0.000 claims 8
- 238000000034 method Methods 0.000 claims 8
- 239000003960 organic solvent Substances 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 3
- -1 3,4-dimethoxyphenyl amine amine Chemical class 0.000 claims 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims 2
- 229910000288 alkali metal carbonate Inorganic materials 0.000 claims 2
- 150000008041 alkali metal carbonates Chemical class 0.000 claims 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- YOUNXJAJHCCMNK-UHFFFAOYSA-N 2-(3,4-diethoxyphenyl)ethanamine Chemical compound CCOC1=CC=C(CCN)C=C1OCC YOUNXJAJHCCMNK-UHFFFAOYSA-N 0.000 claims 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 claims 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims 1
- 239000000920 calcium hydroxide Substances 0.000 claims 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 238000009833 condensation Methods 0.000 claims 1
- 238000006482 condensation reaction Methods 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 229910000027 potassium carbonate Inorganic materials 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims 1
- 235000017557 sodium bicarbonate Nutrition 0.000 claims 1
- 229910000029 sodium carbonate Inorganic materials 0.000 claims 1
- 239000012453 solvate Substances 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C221/00—Preparation of compounds containing amino groups and doubly-bound oxygen atoms bound to the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C225/00—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
- C07C225/02—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to acyclic carbon atoms of the carbon skeleton
- C07C225/14—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being unsaturated
- C07C225/16—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/54—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C217/56—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
- C07C217/60—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms linked by carbon chains having two carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
내용 없음.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (8)
- 구조식(II)의 할로게노 아세토페논 유도체를 산수용체 존재하의 비친수성 유기용매와 물의 2상 용매계에서 3,4-디메톡시펜에 틸아민파 축합시키고 필요하면 그 산물을 산부가염으로 전환시키는 것으로 구성되는 구조식(I)의 아세토페논 유도체나 그의 산부가염을 제조하는 발법.상기 구조식에서 R은 히드록시기의 보호기이고 X는 할로겐원자이다.
- 제1항에 있어서, 비 친수성 유기 용매가 방향족 탄화수소, 할로게노탄화수소, 에테르로 구성되는 기에서 선택되고, 산수용체가 알칼리금속 수산화물, 알칼리 금속 수산화물, 알칼리 금속탄산염, 알칼리 금속중 탄산염으로 구성되는 기에서 선택되는 방법.
- 제1항에 있어서, 비 친수성 유기 용매가 벤젠, 톨루엔, 염화메틸렌, 클로로포름, 디에틸 에테르나 디이소프로필에테르이고, 산 수용체가 수산화나트륨, 수산화 칼륨, 수산화칼슘, 탄산나트륨, 탄산칼륨, 중탄산나트륨인 방법.
- 제1항 내지 제3항중 어느하나에 있어서, 축압반응이 0℃-실온에서 수행되는 방법.
- 제4항에 있어서, 축합반응이 0℃-10℃에서 수행되는 방법.
- 제1항 내지 제3항에 있어서, 비친수 성유기용매가 화합물(II)를 용매하기에 충분한 만큼의 양이 사용되고, 물이 산 수용체를 용해하기에 충분한 양이 사용되는 방법.
- 제1항 내지 제3항에 있어서, 화합물(II) 1mole 당 3,4-디에톡시펜에틸아민 1.2-2mole, 화합물(II)중량부당 비 친수성 유기용매 5-10 체적부, 화합물(II) 1mole 당 산 수용체 1.1-3mole을 각각 사용하는 방법.
- 제6항에 있어서, 산 수용체 중량부당 2중량부의 물을 사용하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56200536A JPS58103344A (ja) | 1981-12-11 | 1981-12-11 | アセトフエノン誘導体の製造法 |
JP200536 | 1981-12-11 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR840002770A true KR840002770A (ko) | 1984-07-16 |
KR870000247B1 KR870000247B1 (ko) | 1987-02-21 |
Family
ID=16425933
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR8205547A KR870000247B1 (ko) | 1981-12-11 | 1982-12-10 | 아세토페논 유도체의 제조방법 |
Country Status (10)
Country | Link |
---|---|
JP (1) | JPS58103344A (ko) |
KR (1) | KR870000247B1 (ko) |
AT (1) | AT382613B (ko) |
CA (1) | CA1211126A (ko) |
CH (1) | CH649759A5 (ko) |
DK (1) | DK158643C (ko) |
ES (1) | ES518106A0 (ko) |
HU (1) | HU187806B (ko) |
IT (1) | IT1191242B (ko) |
SE (1) | SE454776B (ko) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW200740779A (en) | 2005-07-22 | 2007-11-01 | Mitsubishi Pharma Corp | Intermediate compound for synthesizing pharmaceutical agent and production method thereof |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2784193A (en) * | 1955-01-19 | 1957-03-05 | Merck & Co Inc | Phenalkylamines |
AU501137B2 (en) * | 1975-12-11 | 1979-06-14 | Tanabe Seiyaku Co., Ltd. | Benzyl alcohol derivatives |
-
1981
- 1981-12-11 JP JP56200536A patent/JPS58103344A/ja active Granted
-
1982
- 1982-12-08 CH CH7143/82A patent/CH649759A5/de not_active IP Right Cessation
- 1982-12-08 CA CA000417254A patent/CA1211126A/en not_active Expired
- 1982-12-10 DK DK550482A patent/DK158643C/da not_active IP Right Cessation
- 1982-12-10 ES ES518106A patent/ES518106A0/es active Granted
- 1982-12-10 SE SE8207080A patent/SE454776B/sv not_active IP Right Cessation
- 1982-12-10 AT AT0449782A patent/AT382613B/de not_active IP Right Cessation
- 1982-12-10 HU HU823990A patent/HU187806B/hu not_active IP Right Cessation
- 1982-12-10 KR KR8205547A patent/KR870000247B1/ko active
- 1982-12-13 IT IT68462/82A patent/IT1191242B/it active
Also Published As
Publication number | Publication date |
---|---|
DK158643B (da) | 1990-06-25 |
DK550482A (da) | 1983-06-12 |
IT8268462A0 (it) | 1982-12-13 |
DK158643C (da) | 1990-11-19 |
ATA449782A (de) | 1986-08-15 |
JPS6335619B2 (ko) | 1988-07-15 |
SE8207080L (sv) | 1983-06-12 |
KR870000247B1 (ko) | 1987-02-21 |
ES8402256A1 (es) | 1984-01-16 |
ES518106A0 (es) | 1984-01-16 |
CH649759A5 (en) | 1985-06-14 |
CA1211126A (en) | 1986-09-09 |
SE454776B (sv) | 1988-05-30 |
SE8207080D0 (sv) | 1982-12-10 |
IT1191242B (it) | 1988-02-24 |
AT382613B (de) | 1987-03-25 |
JPS58103344A (ja) | 1983-06-20 |
HU187806B (en) | 1986-02-28 |
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