CS201537B2 - Process for preparing /n-/mercaptomethyl/phthalimid/-s-/o,o-dimethylphosphorodithioate - Google Patents
Process for preparing /n-/mercaptomethyl/phthalimid/-s-/o,o-dimethylphosphorodithioate Download PDFInfo
- Publication number
- CS201537B2 CS201537B2 CS761573A CS157376A CS201537B2 CS 201537 B2 CS201537 B2 CS 201537B2 CS 761573 A CS761573 A CS 761573A CS 157376 A CS157376 A CS 157376A CS 201537 B2 CS201537 B2 CS 201537B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- mixture
- hydroxymethylphthalimide
- reaction
- organic solvent
- kgmol
- Prior art date
Links
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 title claims 3
- 238000004519 manufacturing process Methods 0.000 title abstract description 13
- CZGGKXNYNPJFAX-UHFFFAOYSA-N Dimethyldithiophosphate Chemical compound COP(S)(=S)OC CZGGKXNYNPJFAX-UHFFFAOYSA-N 0.000 title description 4
- 238000000034 method Methods 0.000 claims abstract description 49
- 238000006243 chemical reaction Methods 0.000 claims abstract description 44
- 239000002904 solvent Substances 0.000 claims abstract description 18
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 60
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 35
- MNSGOOCAMMSKGI-UHFFFAOYSA-N N-(hydroxymethyl)phthalimide Chemical compound C1=CC=C2C(=O)N(CO)C(=O)C2=C1 MNSGOOCAMMSKGI-UHFFFAOYSA-N 0.000 claims description 34
- 239000003960 organic solvent Substances 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 22
- JKGLRGGCGUQNEX-UHFFFAOYSA-N 2-(chloromethyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCl)C(=O)C2=C1 JKGLRGGCGUQNEX-UHFFFAOYSA-N 0.000 claims description 20
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims description 16
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims description 16
- 239000012074 organic phase Substances 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 238000002360 preparation method Methods 0.000 claims description 7
- 239000011541 reaction mixture Substances 0.000 claims description 7
- KOITVPOIFJTHPW-UHFFFAOYSA-N 2-(sulfanylmethyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CS)C(=O)C2=C1 KOITVPOIFJTHPW-UHFFFAOYSA-N 0.000 claims description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- LMNZTLDVJIUSHT-UHFFFAOYSA-N phosmet Chemical compound C1=CC=C2C(=O)N(CSP(=S)(OC)OC)C(=O)C2=C1 LMNZTLDVJIUSHT-UHFFFAOYSA-N 0.000 abstract 2
- 239000000047 product Substances 0.000 description 17
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- -1 ester phosphorodithioate Chemical class 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000008346 aqueous phase Substances 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000012065 filter cake Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000005191 phase separation Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 102100023904 Nuclear autoantigenic sperm protein Human genes 0.000 description 1
- 101710149564 Nuclear autoantigenic sperm protein Proteins 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000012455 biphasic mixture Substances 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- NAGJZTKCGNOGPW-UHFFFAOYSA-K dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [O-]P([O-])([S-])=S NAGJZTKCGNOGPW-UHFFFAOYSA-K 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- XMYQHJDBLRZMLW-UHFFFAOYSA-N methanolamine Chemical compound NCO XMYQHJDBLRZMLW-UHFFFAOYSA-N 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 238000003260 vortexing Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/5537—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom the heteroring containing the structure -C(=O)-N-C(=O)- (both carbon atoms belong to the heteroring)
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Indole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS79596A CS201536B2 (cs) | 1975-03-10 | 1979-01-26 | Způsob výroby N-ehlormethylftalimidu |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/557,002 US4013685A (en) | 1975-03-10 | 1975-03-10 | Process for the manufacture of n(mercaptomethyl) phthalimide s-(o,o-dimethyl phosphorodithioate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS201537B2 true CS201537B2 (en) | 1980-11-28 |
Family
ID=24223672
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS761573A CS201537B2 (en) | 1975-03-10 | 1976-03-10 | Process for preparing /n-/mercaptomethyl/phthalimid/-s-/o,o-dimethylphosphorodithioate |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US4013685A (ja) |
| JP (1) | JPS51108063A (ja) |
| AU (1) | AU1054676A (ja) |
| BE (1) | BE839213A (ja) |
| BG (2) | BG26525A4 (ja) |
| BR (1) | BR7600985A (ja) |
| CA (1) | CA1057293A (ja) |
| CH (1) | CH626064A5 (ja) |
| CS (1) | CS201537B2 (ja) |
| DD (1) | DD126602A5 (ja) |
| DE (1) | DE2607825A1 (ja) |
| DK (1) | DK141072B (ja) |
| ES (1) | ES445911A1 (ja) |
| FR (1) | FR2303800A1 (ja) |
| GB (1) | GB1487038A (ja) |
| HU (1) | HU174831B (ja) |
| IL (1) | IL48886A (ja) |
| IN (2) | IN144856B (ja) |
| IT (1) | IT1057937B (ja) |
| NL (1) | NL7601186A (ja) |
| NZ (1) | NZ179813A (ja) |
| PH (1) | PH12871A (ja) |
| PL (2) | PL104430B1 (ja) |
| RO (1) | RO76089A (ja) |
| SU (1) | SU652897A3 (ja) |
| TR (1) | TR18734A (ja) |
| ZA (1) | ZA76450B (ja) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3347913A1 (de) * | 1983-03-25 | 1985-06-27 | LuK Lamellen und Kupplungsbau GmbH, 7580 Bühl | Reibungskupplung |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2767194A (en) * | 1955-03-18 | 1956-10-16 | Stauffer Chemical Co | Compositions of matter |
-
1975
- 1975-03-10 US US05/557,002 patent/US4013685A/en not_active Expired - Lifetime
-
1976
- 1976-01-21 IL IL48886A patent/IL48886A/xx unknown
- 1976-01-22 NZ NZ179813A patent/NZ179813A/xx unknown
- 1976-01-23 AU AU10546/76A patent/AU1054676A/en not_active Expired
- 1976-01-27 GB GB3049/76A patent/GB1487038A/en not_active Expired
- 1976-01-27 ZA ZA450A patent/ZA76450B/xx unknown
- 1976-02-03 JP JP51010081A patent/JPS51108063A/ja active Pending
- 1976-02-05 NL NL7601186A patent/NL7601186A/xx not_active Application Discontinuation
- 1976-02-06 IN IN213/CAL/76A patent/IN144856B/en unknown
- 1976-02-11 CA CA245,523A patent/CA1057293A/en not_active Expired
- 1976-02-12 DK DK57876AA patent/DK141072B/da not_active IP Right Cessation
- 1976-02-17 BR BR7600985A patent/BR7600985A/pt unknown
- 1976-02-26 DE DE19762607825 patent/DE2607825A1/de not_active Withdrawn
- 1976-02-26 SU SU762325152A patent/SU652897A3/ru active
- 1976-03-03 PH PH18167A patent/PH12871A/en unknown
- 1976-03-04 BE BE7000791A patent/BE839213A/xx not_active IP Right Cessation
- 1976-03-05 CH CH278676A patent/CH626064A5/de not_active IP Right Cessation
- 1976-03-05 FR FR7606295A patent/FR2303800A1/fr active Granted
- 1976-03-08 IT IT48449/76A patent/IT1057937B/it active
- 1976-03-09 HU HU76SA2898A patent/HU174831B/hu unknown
- 1976-03-09 ES ES445911A patent/ES445911A1/es not_active Expired
- 1976-03-09 TR TR18734A patent/TR18734A/xx unknown
- 1976-03-10 CS CS761573A patent/CS201537B2/cs unknown
- 1976-03-10 BG BG7633633A patent/BG26525A4/xx unknown
- 1976-03-10 PL PL1976200091A patent/PL104430B1/pl unknown
- 1976-03-10 PL PL1976187820A patent/PL98622B1/pl unknown
- 1976-03-10 BG BG7632576A patent/BG26524A3/xx unknown
- 1976-03-10 DD DD191779A patent/DD126602A5/xx unknown
- 1976-03-30 RO RO7684982A patent/RO76089A/ro unknown
-
1977
- 1977-04-19 IN IN596/CAL/77A patent/IN145005B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TR18734A (tr) | 1977-07-27 |
| DD126602A5 (ja) | 1977-08-03 |
| CA1057293A (en) | 1979-06-26 |
| SU652897A3 (ru) | 1979-03-15 |
| AU1054676A (en) | 1977-07-28 |
| IL48886A (en) | 1980-10-26 |
| IL48886A0 (en) | 1976-03-31 |
| DK57876A (ja) | 1976-09-11 |
| BG26525A4 (ja) | 1979-04-12 |
| IN144856B (ja) | 1978-07-15 |
| DK141072B (da) | 1980-01-07 |
| NZ179813A (en) | 1978-04-03 |
| FR2303800A1 (fr) | 1976-10-08 |
| US4013685A (en) | 1977-03-22 |
| IT1057937B (it) | 1982-03-30 |
| GB1487038A (en) | 1977-09-28 |
| BG26524A3 (ja) | 1979-04-12 |
| DK141072C (ja) | 1980-06-16 |
| PL104430B1 (pl) | 1979-08-31 |
| PL98622B1 (pl) | 1978-05-31 |
| ES445911A1 (es) | 1977-11-01 |
| RO76089A (ro) | 1981-04-30 |
| NL7601186A (nl) | 1976-09-14 |
| CH626064A5 (ja) | 1981-10-30 |
| DE2607825A1 (de) | 1976-09-23 |
| PH12871A (en) | 1979-09-25 |
| IN145005B (ja) | 1978-08-12 |
| ZA76450B (en) | 1977-01-26 |
| HU174831B (hu) | 1980-03-28 |
| JPS51108063A (ja) | 1976-09-25 |
| BE839213A (nl) | 1976-09-06 |
| FR2303800B1 (ja) | 1982-01-29 |
| BR7600985A (pt) | 1976-09-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0045290B1 (en) | Continuous process for the production of peroxycarboxylic acid compositions | |
| PL210148B1 (pl) | Sposób wytwarzania sulfonamidu | |
| CS201537B2 (en) | Process for preparing /n-/mercaptomethyl/phthalimid/-s-/o,o-dimethylphosphorodithioate | |
| SU535910A3 (ru) | Способ получени трис-(2-хлорэтил) фосфита | |
| EP0092117B1 (en) | Process for producing chloronicotinic acid compounds | |
| US4185053A (en) | Process for manufacturing substantially pure dialkyl phosphorochloridothionate | |
| US2839554A (en) | Esters of antimony | |
| CS201536B2 (cs) | Způsob výroby N-ehlormethylftalimidu | |
| US4025586A (en) | Preparation of dialkyl phosphorochloridothioates | |
| US2763683A (en) | Preparation of salicylanilide | |
| US4554368A (en) | Continuous process for the preparation of alkyltin thiocarboxylic acid esters | |
| CA1238050A (en) | Continuous process for the preparation of alkyltin thiocarboxylic acid esters | |
| US3991110A (en) | Preparation of hexamethylphosphoramide | |
| JP2558497B2 (ja) | アルキルジハロゲノホスファンの製造法 | |
| US4209471A (en) | Process for the purification of O,O-di(lower)alkyldithiophosphoric acids | |
| US3590104A (en) | Process for preparing 0,0-dialkyl-0-phenyl phosphorothioates | |
| JPH0475220B2 (ja) | ||
| US4877901A (en) | Process for synthesizing N,N'-dithiobis(sulfonamides) | |
| US3931294A (en) | Production of 2-phenyl-ethylene phosphonic acid | |
| EP0048172B1 (en) | Process for producing dialkyl phosphorochloridothionates | |
| KR930006194B1 (ko) | α-클로로아세토아세트산 모노메틸아미드의 제조방법 | |
| JPS647060B2 (ja) | ||
| US2766248A (en) | Process for the production of alkyl pyridines | |
| SU906371A3 (ru) | Способ получени галогенангидридов @ -галогеналкилкарбаминовой кислоты | |
| CA1082878A (en) | Process for preparing high cyclic phosphonitrilic halides |