IL108189A - 4-Hydroxy-2'-nitrobutyrophenone and tetrahydro-2-(0-nitrophenyl)- 2-furanol useful as intermediates in the preparation of a cropselective herbicide - Google Patents
4-Hydroxy-2'-nitrobutyrophenone and tetrahydro-2-(0-nitrophenyl)- 2-furanol useful as intermediates in the preparation of a cropselective herbicideInfo
- Publication number
- IL108189A IL108189A IL10818993A IL10818993A IL108189A IL 108189 A IL108189 A IL 108189A IL 10818993 A IL10818993 A IL 10818993A IL 10818993 A IL10818993 A IL 10818993A IL 108189 A IL108189 A IL 108189A
- Authority
- IL
- Israel
- Prior art keywords
- nitrobutyrophenone
- nitrophenyl
- tetrahydro
- hydroxy
- solvent
- Prior art date
Links
- FWJBSIHKBKEPQX-UHFFFAOYSA-N 4-hydroxy-1-(2-nitrophenyl)butan-1-one Chemical compound OCCCC(=O)C1=CC=CC=C1[N+]([O-])=O FWJBSIHKBKEPQX-UHFFFAOYSA-N 0.000 title claims abstract description 15
- 238000002360 preparation method Methods 0.000 title claims description 11
- 239000004009 herbicide Substances 0.000 title description 6
- 239000000543 intermediate Substances 0.000 title description 5
- 230000002363 herbicidal effect Effects 0.000 title description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims abstract description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 16
- WBEMUPAQEAUPKF-UHFFFAOYSA-N 2-(2-nitrophenyl)oxolan-2-ol Chemical compound C=1C=CC=C([N+]([O-])=O)C=1C1(O)CCCO1 WBEMUPAQEAUPKF-UHFFFAOYSA-N 0.000 claims abstract description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 15
- 239000002904 solvent Substances 0.000 claims abstract description 12
- 229910000039 hydrogen halide Inorganic materials 0.000 claims abstract description 10
- 239000012433 hydrogen halide Substances 0.000 claims abstract description 10
- 239000003960 organic solvent Substances 0.000 claims abstract description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims abstract description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000003444 phase transfer catalyst Substances 0.000 claims abstract description 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims abstract description 6
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims abstract description 5
- NDKBVBUGCNGSJJ-UHFFFAOYSA-M benzyltrimethylammonium hydroxide Chemical group [OH-].C[N+](C)(C)CC1=CC=CC=C1 NDKBVBUGCNGSJJ-UHFFFAOYSA-M 0.000 claims abstract description 4
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims abstract description 3
- 229910052801 chlorine Inorganic materials 0.000 claims abstract 3
- 239000000203 mixture Substances 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 15
- 150000001875 compounds Chemical class 0.000 claims description 13
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical group Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical group Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 239000011877 solvent mixture Substances 0.000 claims description 3
- 229910000042 hydrogen bromide Inorganic materials 0.000 claims description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 2
- 150000002367 halogens Chemical group 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 239000011260 aqueous acid Substances 0.000 claims 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
- HJJMZFWWAYITCI-UHFFFAOYSA-N 3-(2-nitrobenzoyl)oxolan-2-one Chemical compound [O-][N+](=O)C1=CC=CC=C1C(=O)C1C(=O)OCC1 HJJMZFWWAYITCI-UHFFFAOYSA-N 0.000 abstract description 3
- 239000002253 acid Substances 0.000 abstract description 2
- 125000000217 alkyl group Chemical group 0.000 abstract description 2
- 125000001475 halogen functional group Chemical group 0.000 abstract description 2
- 239000001117 sulphuric acid Substances 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 238000010586 diagram Methods 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 229940073584 methylene chloride Drugs 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- ZWRLWJAFBLTMSQ-UHFFFAOYSA-N Docosa-7,10,14-triensaeure Natural products C1C(C)=C2CC(C)(C)CC2C(O)C2=COC=C21 ZWRLWJAFBLTMSQ-UHFFFAOYSA-N 0.000 description 3
- 125000006255 cyclopropyl carbonyl group Chemical group [H]C1([H])C([H])([H])C1([H])C(*)=O 0.000 description 3
- YKASHPSKFYVZRC-UHFFFAOYSA-M furan-2-ylmethyl(trimethyl)azanium;iodide Chemical compound [I-].C[N+](C)(C)CC1=CC=CO1 YKASHPSKFYVZRC-UHFFFAOYSA-M 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 2
- WFAULHLDTDDABL-UHFFFAOYSA-N Proxazole citrate Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O.C=1C=CC=CC=1C(CC)C1=NOC(CCN(CC)CC)=N1 WFAULHLDTDDABL-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- VDZOOKBUILJEDG-UHFFFAOYSA-M tetrabutylammonium hydroxide Chemical compound [OH-].CCCC[N+](CCCC)(CCCC)CCCC VDZOOKBUILJEDG-UHFFFAOYSA-M 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- HMOJKUDFFLOQTN-UHFFFAOYSA-N (2-aminophenyl)-cyclopropylmethanone Chemical compound NC1=CC=CC=C1C(=O)C1CC1 HMOJKUDFFLOQTN-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- LDLCZOVUSADOIV-UHFFFAOYSA-N 2-bromoethanol Chemical compound OCCBr LDLCZOVUSADOIV-UHFFFAOYSA-N 0.000 description 1
- FQKYTBQZPFRTDH-UHFFFAOYSA-N 2-hydroxy-1-phenylbutan-1-one Chemical compound CCC(O)C(=O)C1=CC=CC=C1 FQKYTBQZPFRTDH-UHFFFAOYSA-N 0.000 description 1
- VSDZBKACHGJLHP-UHFFFAOYSA-N 4-chloro-1-(2-nitrophenyl)butan-1-one Chemical compound [O-][N+](=O)C1=CC=CC=C1C(=O)CCCCl VSDZBKACHGJLHP-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-OUBTZVSYSA-N Carbon-13 Chemical compound [13C] OKTJSMMVPCPJKN-OUBTZVSYSA-N 0.000 description 1
- 241000722731 Carex Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- -1 alkyl 2-(o-nitrobenzoyl)-acetate compound Chemical class 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- FFSAXUULYPJSKH-UHFFFAOYSA-N butyrophenone Chemical compound CCCC(=O)C1=CC=CC=C1 FFSAXUULYPJSKH-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- OWZNCVIBJQPNEF-UHFFFAOYSA-N ethyl 3-(2-nitrophenyl)-3-oxopropanoate Chemical compound CCOC(=O)CC(=O)C1=CC=CC=C1[N+]([O-])=O OWZNCVIBJQPNEF-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- APVPOHHVBBYQAV-UHFFFAOYSA-N n-(4-aminophenyl)sulfonyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 APVPOHHVBBYQAV-UHFFFAOYSA-N 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229940073455 tetraethylammonium hydroxide Drugs 0.000 description 1
- LRGJRHZIDJQFCL-UHFFFAOYSA-M tetraethylazanium;hydroxide Chemical compound [OH-].CC[N+](CC)(CC)CC LRGJRHZIDJQFCL-UHFFFAOYSA-M 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/18—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/20—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/45—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by at least one doubly—bound oxygen atom, not being part of a —CHO group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Furan Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/997,844 US5281726A (en) | 1992-12-29 | 1992-12-29 | 4-hydroxy-2'-nitrobutyrophenone and tetrahydro-2-(o-nitrophenyl)-2-furanol useful as intermediates in the preparation of a crop-selective herbicide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL108189A0 IL108189A0 (en) | 1994-04-12 |
| IL108189A true IL108189A (en) | 1998-07-15 |
Family
ID=25544466
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL10818993A IL108189A (en) | 1992-12-29 | 1993-12-27 | 4-Hydroxy-2'-nitrobutyrophenone and tetrahydro-2-(0-nitrophenyl)- 2-furanol useful as intermediates in the preparation of a cropselective herbicide |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US5281726A (cs) |
| EP (1) | EP0604705B1 (cs) |
| JP (1) | JP3488928B2 (cs) |
| KR (1) | KR970006886B1 (cs) |
| CN (1) | CN1055678C (cs) |
| AT (1) | ATE143940T1 (cs) |
| AU (1) | AU671165B2 (cs) |
| BR (1) | BR9305256A (cs) |
| CA (1) | CA2112414C (cs) |
| CZ (2) | CZ285520B6 (cs) |
| DE (1) | DE69305314T2 (cs) |
| DK (1) | DK0604705T3 (cs) |
| ES (1) | ES2092734T3 (cs) |
| HK (1) | HK1001051A1 (cs) |
| HU (1) | HU213252B (cs) |
| IL (1) | IL108189A (cs) |
| MX (1) | MX9307492A (cs) |
| SG (1) | SG47558A1 (cs) |
| SK (1) | SK279439B6 (cs) |
| TW (1) | TW235292B (cs) |
| ZA (1) | ZA939739B (cs) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6127576A (en) * | 1996-12-20 | 2000-10-03 | American Cyanamid Company | Aminophenyl ketone derivatives and a method for the preparation thereof |
| TW434205B (en) * | 1997-01-06 | 2001-05-16 | American Cyanamid Co | Aryne intermediates and a process for the preparation thereof |
| US5856576A (en) * | 1997-02-04 | 1999-01-05 | American Cyanamid Company | Aryne intermediates and a process for the preparation thereof |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3562277A (en) | 1967-09-06 | 1971-02-09 | Shulton Inc | Ketonic derivatives of phenyl piperazines |
| FI60559C (fi) * | 1975-07-17 | 1982-02-10 | Sumitomo Chemical Co | Foerfarande foer framstaellning av ny-(tertiaer amino)-orto-aminobutyrofenonfoereningar |
| US5009699A (en) * | 1990-06-22 | 1991-04-23 | American Cyanamid Company | 1-{[O-(cyclopropylcarbonyl)phenyl]sulfamoyl}-3-(4,6-dimethoxy-2-pyrimidinyl)urea herbicidal composition and use |
-
1992
- 1992-12-29 US US07/997,844 patent/US5281726A/en not_active Expired - Lifetime
-
1993
- 1993-08-05 DK DK93112564.5T patent/DK0604705T3/da active
- 1993-08-05 EP EP93112564A patent/EP0604705B1/en not_active Expired - Lifetime
- 1993-08-05 DE DE69305314T patent/DE69305314T2/de not_active Expired - Lifetime
- 1993-08-05 SG SG1996002822A patent/SG47558A1/en unknown
- 1993-08-05 ES ES93112564T patent/ES2092734T3/es not_active Expired - Lifetime
- 1993-08-05 AT AT93112564T patent/ATE143940T1/de not_active IP Right Cessation
- 1993-08-16 TW TW082106572A patent/TW235292B/zh active
- 1993-10-22 CN CN93119057A patent/CN1055678C/zh not_active Expired - Fee Related
- 1993-11-29 MX MX9307492A patent/MX9307492A/es not_active IP Right Cessation
- 1993-12-15 CZ CZ932762A patent/CZ285520B6/cs not_active IP Right Cessation
- 1993-12-15 CZ CZ984373A patent/CZ285777B6/cs not_active IP Right Cessation
- 1993-12-21 SK SK1460-93A patent/SK279439B6/sk unknown
- 1993-12-22 JP JP34554493A patent/JP3488928B2/ja not_active Expired - Fee Related
- 1993-12-24 CA CA002112414A patent/CA2112414C/en not_active Expired - Fee Related
- 1993-12-24 AU AU52678/93A patent/AU671165B2/en not_active Ceased
- 1993-12-27 IL IL10818993A patent/IL108189A/en active IP Right Grant
- 1993-12-28 KR KR1019930030415A patent/KR970006886B1/ko not_active Expired - Fee Related
- 1993-12-28 ZA ZA939739A patent/ZA939739B/xx unknown
- 1993-12-28 BR BR9305256A patent/BR9305256A/pt not_active Application Discontinuation
- 1993-12-28 HU HU9303773A patent/HU213252B/hu not_active IP Right Cessation
-
1998
- 1998-01-05 HK HK98100068A patent/HK1001051A1/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CZ285777B6 (cs) | 1999-11-17 |
| CN1055678C (zh) | 2000-08-23 |
| EP0604705B1 (en) | 1996-10-09 |
| AU5267893A (en) | 1994-07-14 |
| CA2112414A1 (en) | 1994-06-30 |
| SG47558A1 (en) | 1998-04-17 |
| HU213252B (en) | 1997-04-28 |
| ZA939739B (en) | 1994-08-18 |
| CZ276293A3 (en) | 1994-07-13 |
| JPH06199742A (ja) | 1994-07-19 |
| AU671165B2 (en) | 1996-08-15 |
| HU9303773D0 (en) | 1994-04-28 |
| KR970006886B1 (ko) | 1997-04-30 |
| TW235292B (cs) | 1994-12-01 |
| DE69305314D1 (de) | 1996-11-14 |
| IL108189A0 (en) | 1994-04-12 |
| CA2112414C (en) | 2004-01-27 |
| SK279439B6 (sk) | 1998-11-04 |
| DK0604705T3 (da) | 1996-11-18 |
| CZ285520B6 (cs) | 1999-08-11 |
| HUT66564A (en) | 1994-12-28 |
| MX9307492A (es) | 1994-08-31 |
| DE69305314T2 (de) | 1997-03-06 |
| ATE143940T1 (de) | 1996-10-15 |
| US5281726A (en) | 1994-01-25 |
| CN1088910A (zh) | 1994-07-06 |
| KR940014295A (ko) | 1994-07-18 |
| SK146093A3 (en) | 1994-12-07 |
| ES2092734T3 (es) | 1996-12-01 |
| HK1001051A1 (en) | 1998-05-22 |
| JP3488928B2 (ja) | 2004-01-19 |
| EP0604705A1 (en) | 1994-07-06 |
| BR9305256A (pt) | 1994-11-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FF | Patent granted | ||
| KB | Patent renewed | ||
| KB | Patent renewed |