GB1306868A - Fatty ethers - Google Patents
Fatty ethersInfo
- Publication number
- GB1306868A GB1306868A GB4420470A GB4420470A GB1306868A GB 1306868 A GB1306868 A GB 1306868A GB 4420470 A GB4420470 A GB 4420470A GB 4420470 A GB4420470 A GB 4420470A GB 1306868 A GB1306868 A GB 1306868A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polyhydric alcohol
- carbon atoms
- radical
- compound
- formula
- 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
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- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/04—Saturated ethers
- C07C43/13—Saturated ethers containing hydroxy or O-metal groups
- C07C43/135—Saturated ethers containing hydroxy or O-metal groups having more than one ether bond
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/024—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings having at least two phenol groups but no condensed ring
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- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1306868 Fatty polyethers ATLAS CHEMICAL INDUSTRIES Inc 16 Sept 1970 [17 Sept 1969 (2)] 44204/70 Heading C2C [Also in Divisions C3 and C5] The invention comprises compounds of the formula [R-X-R 2 -O]y-R 3 (1) where R is alkyl, alkenyl, alkaryl or alkenaryl; y is 1, 2, 3 or 4; X is -S-, -O- or -CH 2 -; R 2 is - CH 2 H(CH 2 OH)- or -CH 2 CH( OH )CH 2 - the radical R-X-R 2 containing a saturated or unsaturated aliphatic hydrocarbon chain, of at least 8 carbon atoms, and R 3 is the radical which remains when y hydroxyl groups are removed from a polyhydric alcohol anhydride which contains at least one hydroxyl group and at least 4 carbon atoms or a polyalkyleneoxy derivative thereof, and compositions comprising at least 10% of a compound of the Formula (1) above and a compound of the formula where R 1 is the radical which remains when y hydroxyl groups are removed from a polyhydric alcohol containing at least 3 carbon atoms and 3 hydroxyl groups, the compositions not containing more than 10 wt. per cent of ethers derived from polyhydric alcohols of 3 carbon atoms, and their preparation by reacting a compound R-X-R 4 , where R 4 is an oxiranylmethyl radical with a polyhydric alcohol anhydride or an oxyalkylene derivative thereof and a polyhydric alcohol, the reaction being carried out in the presence of an epoxide addition catalyst, in such a manner as to provide 1-6 mols. epoxide per mol. polyhydric alcohol anhydride and polyhydric alcohol. The polyols from which R 3 is derived are preferably APolyols made by hydrogenolysing sugars and distilling the reduced product. The polyols are dehydrated under acid or basic conditions to give the polyol anhydrides. The epoxides R-X-R 4 may be made by reacting an alcohol or thiol R-XH with epiehlorohydrin, where X is -O- or -S-.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US85888169A | 1969-09-17 | 1969-09-17 | |
US85888769A | 1969-09-17 | 1969-09-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1306868A true GB1306868A (en) | 1973-02-14 |
Family
ID=27127486
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4420470A Expired GB1306868A (en) | 1969-09-17 | 1970-09-16 | Fatty ethers |
Country Status (2)
Country | Link |
---|---|
FR (1) | FR2062278A5 (en) |
GB (1) | GB1306868A (en) |
-
1970
- 1970-09-16 GB GB4420470A patent/GB1306868A/en not_active Expired
- 1970-09-17 FR FR7033771A patent/FR2062278A5/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR2062278A5 (en) | 1971-06-25 |
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Legal Events
Date | Code | Title | Description |
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PS | Patent sealed | ||
PE20 | Patent expired after termination of 20 years |