GB736448A - Process of producing tertiary phosphoric acid esters of partial carboxylic acid esters of polyhydric alcohols - Google Patents
Process of producing tertiary phosphoric acid esters of partial carboxylic acid esters of polyhydric alcoholsInfo
- Publication number
- GB736448A GB736448A GB11134/53A GB1113453A GB736448A GB 736448 A GB736448 A GB 736448A GB 11134/53 A GB11134/53 A GB 11134/53A GB 1113453 A GB1113453 A GB 1113453A GB 736448 A GB736448 A GB 736448A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mol
- mols
- ester
- reacted
- acid
- 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
- 150000005846 sugar alcohols Polymers 0.000 title abstract 5
- 150000003014 phosphoric acid esters Chemical group 0.000 title abstract 3
- 150000001733 carboxylic acid esters Chemical class 0.000 title 1
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 abstract 18
- 150000002148 esters Chemical class 0.000 abstract 15
- 238000006243 chemical reaction Methods 0.000 abstract 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 7
- 235000021355 Stearic acid Nutrition 0.000 abstract 6
- 239000000203 mixture Substances 0.000 abstract 6
- 229920001223 polyethylene glycol Polymers 0.000 abstract 6
- -1 ether alcohols Chemical class 0.000 abstract 5
- 239000002202 Polyethylene glycol Substances 0.000 abstract 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 abstract 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract 4
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract 4
- 239000008117 stearic acid Substances 0.000 abstract 4
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 abstract 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 150000007513 acids Chemical class 0.000 abstract 3
- 150000001735 carboxylic acids Chemical class 0.000 abstract 3
- 230000032050 esterification Effects 0.000 abstract 3
- 238000005886 esterification reaction Methods 0.000 abstract 3
- PFSJIJDPXOUPEI-UHFFFAOYSA-N 1-(2-hydroxyethoxy)icosan-2-ol Chemical compound CCCCCCCCCCCCCCCCCCC(O)COCCO PFSJIJDPXOUPEI-UHFFFAOYSA-N 0.000 abstract 2
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 abstract 2
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 abstract 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000005639 Lauric acid Substances 0.000 abstract 2
- 229910019142 PO4 Inorganic materials 0.000 abstract 2
- 150000008064 anhydrides Chemical class 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 238000005238 degreasing Methods 0.000 abstract 2
- 239000003599 detergent Substances 0.000 abstract 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract 2
- 239000003995 emulsifying agent Substances 0.000 abstract 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 abstract 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 abstract 2
- 239000010452 phosphate Substances 0.000 abstract 2
- 238000006068 polycondensation reaction Methods 0.000 abstract 2
- 229920000151 polyglycol Polymers 0.000 abstract 2
- 239000010695 polyglycol Substances 0.000 abstract 2
- 229920001451 polypropylene glycol Polymers 0.000 abstract 2
- 238000004513 sizing Methods 0.000 abstract 2
- 235000011044 succinic acid Nutrition 0.000 abstract 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 abstract 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 abstract 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 abstract 1
- NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 abstract 1
- 150000001991 dicarboxylic acids Chemical class 0.000 abstract 1
- 239000002270 dispersing agent Substances 0.000 abstract 1
- 150000002334 glycols Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- FBPFZTCFMRRESA-UHFFFAOYSA-N hexane-1,2,3,4,5,6-hexol Chemical compound OCC(O)C(O)C(O)C(O)CO FBPFZTCFMRRESA-UHFFFAOYSA-N 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 150000002689 maleic acids Chemical class 0.000 abstract 1
- 239000002674 ointment Substances 0.000 abstract 1
- 235000021313 oleic acid Nutrition 0.000 abstract 1
- 150000002889 oleic acids Chemical class 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- LCPDWSOZIOUXRV-UHFFFAOYSA-N phenoxyacetic acid Chemical class OC(=O)COC1=CC=CC=C1 LCPDWSOZIOUXRV-UHFFFAOYSA-N 0.000 abstract 1
- 229920000223 polyglycerol Polymers 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 239000001384 succinic acid Substances 0.000 abstract 1
- 150000003444 succinic acids Chemical class 0.000 abstract 1
- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical compound O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 abstract 1
- 229940014800 succinic anhydride Drugs 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/091—Esters of phosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
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)
- Lubricants (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE736448X | 1952-05-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB736448A true GB736448A (en) | 1955-09-07 |
Family
ID=6642317
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB11134/53A Expired GB736448A (en) | 1952-05-09 | 1953-04-22 | Process of producing tertiary phosphoric acid esters of partial carboxylic acid esters of polyhydric alcohols |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE519557A (ja) |
| FR (1) | FR1076808A (ja) |
| GB (1) | GB736448A (ja) |
| NL (1) | NL88848C (ja) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3013991A (en) * | 1957-10-09 | 1961-12-19 | Pure Oil Co | Organophosphorus polymers |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2726854A1 (de) * | 1977-06-15 | 1979-01-11 | Bayer Ag | Phosphorsaeureester |
| NO901322L (no) * | 1989-03-27 | 1990-09-28 | Aluminum Co Of America | Smoeremiddel, samt fremgangsmaate for fremstilling av et slikt. |
-
0
- BE BE519557D patent/BE519557A/xx unknown
-
1953
- 1953-03-16 NL NL176883A patent/NL88848C/xx active
- 1953-04-22 GB GB11134/53A patent/GB736448A/en not_active Expired
- 1953-05-09 FR FR1076808D patent/FR1076808A/fr not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3013991A (en) * | 1957-10-09 | 1961-12-19 | Pure Oil Co | Organophosphorus polymers |
Also Published As
| Publication number | Publication date |
|---|---|
| NL88848C (ja) | |
| BE519557A (ja) | |
| FR1076808A (fr) | 1954-10-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69707757T2 (de) | Veresterungsverfahren | |
| US3023183A (en) | Esterification | |
| GB588834A (en) | Stabilisation of polyesters | |
| US3457206A (en) | Water dispersible alkyd resins comprising esterified units of an alkoxypolyoxyethylene glycol | |
| US2151185A (en) | Esters of glycol monoesters and acylated hydroxy acids | |
| GB736448A (en) | Process of producing tertiary phosphoric acid esters of partial carboxylic acid esters of polyhydric alcohols | |
| US3196117A (en) | Intermolecular alkyd-epoxy complexes | |
| US3223658A (en) | Stable aqueous alkyd resin emulsions | |
| US2907736A (en) | Esters of polyhydric phenols | |
| EP0031310B1 (en) | Nonionic surface active monoester and method for its production | |
| JPS6314730B2 (ja) | ||
| US3248404A (en) | Novel epoxidation process | |
| GB977705A (en) | Process for the production of foamed polyester polyurethanes | |
| DE971212C (de) | Verfahren zur Herstellung tertiaerer Phosphorsaeureester partieller Carbonsaeureester mehrwertiger Alkohole | |
| GB1079256A (en) | Improvements in or relating to the manufacture of foamed polyurethanes | |
| US2412176A (en) | Treating fatty oils | |
| US3197439A (en) | Preparation of polyester resins | |
| US2224360A (en) | Process of manufacturing washing, cleansing, wetting, and emulsifying agents | |
| GB620698A (en) | Improvements in and relating to synthetic resinous compositions | |
| JPS6149428B2 (ja) | ||
| GB871291A (en) | Production of hydrophilic polyester-urethane foamed or cellular products | |
| US2913452A (en) | Diamtoes of heterocyclic hydroxy | |
| GB765551A (en) | Manufacture of polysiloxane condensation products | |
| US2307794A (en) | Process for producing synthetic | |
| JPS6028949B2 (ja) | 繊維処理剤 |