GB1378962A - Phosphonic ester derivatives having flame-proofing properties - Google Patents
Phosphonic ester derivatives having flame-proofing propertiesInfo
- Publication number
- GB1378962A GB1378962A GB1382572A GB1382572A GB1378962A GB 1378962 A GB1378962 A GB 1378962A GB 1382572 A GB1382572 A GB 1382572A GB 1382572 A GB1382572 A GB 1382572A GB 1378962 A GB1378962 A GB 1378962A
- Authority
- GB
- United Kingdom
- Prior art keywords
- radical
- polyhydric alcohol
- formula
- formaldehyde
- reacted
- 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
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
- D06M13/282—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
- D06M13/288—Phosphonic or phosphonous acids or derivatives thereof
-
- 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 System
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se)
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
-
- 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 System
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
- C07F9/657163—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom
- C07F9/657181—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom the ring phosphorus atom and, at least, one ring oxygen atom being part of a (thio)phosphonic acid derivative
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)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Fireproofing Substances (AREA)
Abstract
1378962 Phosphonic acid esters BADISCHE ANILIN- & SODA-FABRIK AG 24 March 1972 [26 March 1971] 13825/72 Heading C2P [Also in Division D1] Novel compounds of the formula A(-B) n in which A is the radical of a n-hydric alcohol, n is an integer from 2 to 6 and each B independently is a radical of formula in which R<SP>1</SP> and R<SP>2</SP> are C 1 -C 4 alkyl or together denote a C 2 or C 3 alkylene radical, R<SP>3</SP> is H or C 1 -C 4 alkyl and R<SP>4</SP> is the same or different in any one molecule of the compound and is selected from H atoms, C 1 -C 3 alkyl, methylol or alkoxymethyl with 1 to 4 carbon atoms in the alkoxy group are obtained by reacting a phosphite diester: (R<SP>1</SP>O)(R<SP>2</SP>O)P(O)H with an unsaturated amide: H 2 C=C(R<SP>3</SP>)CONH(R<SP>4</SP>), formaldehyde, and a polyhydric alcohol A(H) n in stoichiometric amounts in any order. Preferred products are those in which A is the radical of a dihydric alcohol of 2 or 3 carbon atoms, R 1 and R 2 are identical and are each CH 3 or C 2 H 5 , R 3 is H, and R<SP>4</SP> is H, CH 3 or -CH 2 OH. The radical A may contain an ether oxygen atom (or atoms) or may be a radical derived from a spatially branched polyhydric alcohol such as pentaerythritol or of, e.g. glycerol or sorbitol. In carrying out the reaction the phosphite diester may be reacted with the unsaturated amide, the resulting product methylolated with formaldehyde and the product then reacted with the polyhydric alcohol or the unsaturated amide may first be methylolated with formaldehyde, the product esterified with the polyhydric alcohol and the resulting product then reacted with the phosphite diester. The compounds may also be obtained directly by reacting a compound of the formula with the phosphite diester suitably in alkaline medium or by etherifying a compound of the formula with a polyhydric alcohol A(H) n suitably in the presence of an acid catalyst. The products are useful for flame-proofing textile material.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19712114610 DE2114610A1 (en) | 1971-03-26 | 1971-03-26 | Derivatives of polyhydric alcohols |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1378962A true GB1378962A (en) | 1975-01-02 |
Family
ID=5802788
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1382572A Expired GB1378962A (en) | 1971-03-26 | 1972-03-24 | Phosphonic ester derivatives having flame-proofing properties |
Country Status (10)
Country | Link |
---|---|
US (1) | US3808292A (en) |
AT (1) | AT312554B (en) |
BE (1) | BE781146A (en) |
CA (1) | CA989412A (en) |
DE (1) | DE2114610A1 (en) |
FR (1) | FR2130369B1 (en) |
GB (1) | GB1378962A (en) |
IT (1) | IT952401B (en) |
NL (1) | NL7204002A (en) |
ZA (1) | ZA722028B (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2331102A1 (en) * | 1973-06-19 | 1975-01-23 | Basf Ag | N- (DIALKYLPHOSPHONOALKYL) -CARBAMIC ACID ALKYLESTER |
US4007318A (en) * | 1975-05-21 | 1977-02-08 | General Electric Company | Phosphorylated polystyrene and method for forming same |
FR2318168A1 (en) * | 1975-07-18 | 1977-02-11 | Produits Ind Cie Fse | NEW PHOSPHONYL AMIDES AND THEIR USE IN FLAME-RESISTANT PROCESSES |
CN103194073B (en) * | 2012-01-09 | 2015-03-11 | 东莞市绿美时环保装饰建材有限公司 | Halogen-free flame-retardant wood-plastic composite material and preparation method thereof |
CN103422772B (en) * | 2012-05-24 | 2015-04-08 | 中国林业科学研究院木材工业研究所 | Wood-plastic composite section and preparation method thereof |
-
1971
- 1971-03-26 DE DE19712114610 patent/DE2114610A1/en active Pending
-
1972
- 1972-03-17 FR FR7209367A patent/FR2130369B1/fr not_active Expired
- 1972-03-20 US US00236203A patent/US3808292A/en not_active Expired - Lifetime
- 1972-03-22 CA CA137,842A patent/CA989412A/en not_active Expired
- 1972-03-23 BE BE781146A patent/BE781146A/en unknown
- 1972-03-24 NL NL7204002A patent/NL7204002A/xx unknown
- 1972-03-24 ZA ZA722028A patent/ZA722028B/en unknown
- 1972-03-24 GB GB1382572A patent/GB1378962A/en not_active Expired
- 1972-03-24 AT AT257272A patent/AT312554B/en not_active IP Right Cessation
- 1972-03-25 IT IT49247/72A patent/IT952401B/en active
Also Published As
Publication number | Publication date |
---|---|
IT952401B (en) | 1973-07-20 |
BE781146A (en) | 1972-09-25 |
CA989412A (en) | 1976-05-18 |
FR2130369A1 (en) | 1972-11-03 |
AT312554B (en) | 1974-01-10 |
FR2130369B1 (en) | 1977-02-11 |
NL7204002A (en) | 1972-09-28 |
ZA722028B (en) | 1973-01-31 |
US3808292A (en) | 1974-04-30 |
DE2114610A1 (en) | 1972-10-05 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed [section 19, patents act 1949] | ||
PLNP | Patent lapsed through nonpayment of renewal fees |