JPS6350336B2 - - Google Patents
Info
- Publication number
- JPS6350336B2 JPS6350336B2 JP20068183A JP20068183A JPS6350336B2 JP S6350336 B2 JPS6350336 B2 JP S6350336B2 JP 20068183 A JP20068183 A JP 20068183A JP 20068183 A JP20068183 A JP 20068183A JP S6350336 B2 JPS6350336 B2 JP S6350336B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- present
- following formula
- formula
- raw material
- 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.)
- Expired
Links
- 150000001875 compounds Chemical class 0.000 claims description 12
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 6
- 150000004967 organic peroxy acids Chemical class 0.000 claims description 6
- 230000002194 synthesizing effect Effects 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 239000002994 raw material Substances 0.000 description 8
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 4
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- -1 alkali metal salt Chemical class 0.000 description 2
- 150000001728 carbonyl compounds Chemical class 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000010189 synthetic method Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 1
- BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- ZKQFHRVKCYFVCN-UHFFFAOYSA-N ethoxyethane;hexane Chemical compound CCOCC.CCCCCC ZKQFHRVKCYFVCN-UHFFFAOYSA-N 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- QPXQVNXSQCRWEV-UHFFFAOYSA-N methoxymethylsulfanylbenzene Chemical compound COCSC1=CC=CC=C1 QPXQVNXSQCRWEV-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
Landscapes
- Pyrane Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20068183A JPS6092233A (ja) | 1983-10-25 | 1983-10-25 | アルデヒドの新規な合成法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20068183A JPS6092233A (ja) | 1983-10-25 | 1983-10-25 | アルデヒドの新規な合成法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6092233A JPS6092233A (ja) | 1985-05-23 |
JPS6350336B2 true JPS6350336B2 (fr) | 1988-10-07 |
Family
ID=16428473
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP20068183A Granted JPS6092233A (ja) | 1983-10-25 | 1983-10-25 | アルデヒドの新規な合成法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6092233A (fr) |
-
1983
- 1983-10-25 JP JP20068183A patent/JPS6092233A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6092233A (ja) | 1985-05-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2556722B2 (ja) | 新規なスルホンアミド化合物 | |
JPH0378395B2 (fr) | ||
JPS6350336B2 (fr) | ||
EP0119091B1 (fr) | Dérivés de l'acide 2,2-diéthoxypropionique | |
US4107181A (en) | Useful prostaglandin intermediates | |
EP0217376B1 (fr) | Procédé pour la fabrication des cétones aryliques alpha-haloalkylés optiquement actives | |
JPH0623176B2 (ja) | 非対称ジチオアセタール及びジチオケタールの製造方法 | |
US5576461A (en) | Preparation of sulphoxonium salts | |
JPH0348909B2 (fr) | ||
US4058567A (en) | Cyclopentene sulfoxides | |
JPS5916879A (ja) | N−置換イミダゾ−ル類の製造法 | |
JP3186416B2 (ja) | 1h−1,2,3−トリアゾ−ルの製法 | |
JPH04316531A (ja) | シクロヘキサノン誘導体 | |
US4052434A (en) | Prostaglandin intermediates | |
JP2005068036A (ja) | 置換ピリドン類の製造方法、その原料化合物およびその製造方法 | |
JP2717997B2 (ja) | 新規ヒドラゾン化合物、及びトリアゾールの製法 | |
HU193454B (en) | Process for producing 3-phenyl-butyraldehyde derivatives | |
US5023382A (en) | Synthesis of 2,3-disubstituted-2-cyclopentenones via lithiomethylmercapto compounds | |
KR0157511B1 (ko) | 2-술포닐티아졸 카르복사미드 유도체의 제조방법 | |
JPS64376B2 (fr) | ||
KR950013853B1 (ko) | 4-에톡시카보닐-i-메틸-5-피라졸머캅탄의 제조방법 | |
US5856511A (en) | Synthesis of 2-(2-furoyl)-4(5)-(2-furanyl)-1H-imidazole and analogs thereof | |
JPH0556350B2 (fr) | ||
JPH06211780A (ja) | ベンゾイルシアナイド誘導体、その製法及びそれを用いた反応 | |
JPH08176134A (ja) | フタリド誘導体の新規な合成方法 |