WO2008088074A1 - β-フェニルエチルアルコールの精製方法 - Google Patents
β-フェニルエチルアルコールの精製方法 Download PDFInfo
- Publication number
- WO2008088074A1 WO2008088074A1 PCT/JP2008/050925 JP2008050925W WO2008088074A1 WO 2008088074 A1 WO2008088074 A1 WO 2008088074A1 JP 2008050925 W JP2008050925 W JP 2008050925W WO 2008088074 A1 WO2008088074 A1 WO 2008088074A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- phenylethyl alcohol
- column
- liquid
- purification
- heavy
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/76—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
- C07C29/80—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by distillation
- C07C29/84—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by distillation by extractive distillation
Definitions
- the present invention relates to a method for purifying / 3-phenylethyl alcohol.
- the present invention selectively separates off-flavor components generated in a purification tower from a single phenyl alcohol efficiently by simple operation without requiring complicated equipment and operation.
- the present invention relates to a method for purifying / 3-phenylethyl alcohol, which is characterized by being capable of obtaining a high-purity ⁇ -phenylethyl alcohol having an excellent aroma for fragrances.
- Phenylethyl alcohol is a valuable substance widely used in detergents, cosmetics, etc., as a rose-based fragrance. For its use, a product with high purity and excellent fragrance is required. In general, special attention is paid to the refining method of perfume ingredients, because even if trace amounts of impurities that affect the original aroma are present, the product value is significantly reduced. In particular, in the purification tower that purifies the final product, the oxidation and dehydration reactions of -phenylethyl alcohol at high temperatures produce phenylacetaldehyde and styrene, which are off-flavor components, and are mixed into the product. There is a topic.
- catalysts for these reactions include organic acids, alkaline catalysts (for example, caustic soda), and air.
- alkaline catalysts for example, caustic soda
- air As a method for purifying 3-phenyl alcohol, which has been reported so far, these catalyst components are separated by simple distillation upstream of the purification tower and then purified (Japanese Patent Laid-Open No. 62-2). 2 8 6 9 3 9) is known.
- these 'methods' have drawbacks and have problems as industrial methods.
- the simple distillation method when the operating pressure of the purification tower is negative, / 3-phenylethyla is generated by the air leaked in a minute amount from the apparatus flange part or the like. There is no effect in suppressing the oxidation reaction of rucol.
- the object of the present invention is to select an off-flavor component produced from 3-phenylethyl alcohol in a purification tower, simply and efficiently, without requiring complicated equipment and operation. And a highly purified / 3-phenylethyl alcohol having an excellent fragrance for a fragrance, and a method for purifying 3-phenylethyl alcohol.
- the present invention is a method for purifying 3-phenylethyl alcohol), wherein 3-phenylethyl alcohol to be purified is supplied to a rectifying column and purified as a side cut)) 3-phenylethyl
- the method relates to a method for purifying monophenyl alcohol that obtains alcohol.
- FIG. 1 is a diagram showing an outline of the flow of the present invention.
- the monophenylethyl alcohol subjected to the purification of the present invention is not particularly limited, and examples thereof include those obtained through the following steps.
- Heavy separation process Crude
- Alkaline washing process A process in which the liquid from which the heavy substance was separated in the heavy separation process is brought into contact with an aqueous alkali
- Light-boiling separation process The process after the alkali washing process is subjected to extractive distillation and liquid-liquid extraction to separate the light-boiling components, and the liquid from which the light-boiling components have been separated is supplied to the rectification column. Is the process of separating heavy components from crude / 3-phenylethyl alcohol.
- Crude-phenylethyl alcohol includes, for example, a method by hydrogen reduction of styrene oxide, a method by reaction of benzene and ethylene oxide, a method by hydrogen reduction of phenylacetic acid, and a method by oxidation reaction of aromatic hydrocarbon compounds. What is obtained can be used.
- the Al force cleaning step is a step in which the liquid separated in the heavy separation step is brought into contact with the Al force aqueous solution.
- the alkaline aqueous solution for example, ammonia water or caustic soda water can be used, and a caustic soda aqueous solution is preferable from the viewpoint of easy handling.
- the alkali concentration of the aqueous alkali solution is usually about 1 to 50% by weight. In order to wash with alkali, it may be crude) 3-phenylethyl alcohol is mixed and contacted with an aqueous alkali solution, and then oil and water are separated.
- the temperature during washing is usually from room temperature (about 20 ° C) to 10 and the amount of alkaline aqueous solution used is 5 to 50 parts by weight with respect to 100 parts by weight of crude 3-phenylethyl alcohol. is there.
- the liquid that has undergone the alkaline cleaning process is subjected to extractive distillation and liquid-liquid extraction to separate the light boiling component, and the liquid separated from the light boiling component is supplied to the rectification column of the present invention.
- the extraction solvent (A) used in the extractive distillation a mixture of water and 1,2-propanediol can be used from the viewpoint of removal efficiency of light boiling components.
- the weight ratio of water to 1,2-propanediol is 1: 9 force, and 7: 3.
- Extractive distillation is carried out under reduced pressure at a temperature of 50 to 200 and under a reflux ratio of 0.1 to 50, and a highly volatile extraction solvent (A) and light boiling components flow out from the top of the column. Then, 0-phenylethyl alcohol from which light-boiling components have been separated and removed is extracted from the bottom of the column.
- A highly volatile extraction solvent
- 0phenylethyl alcohol from which light-boiling components have been separated and removed is extracted from the bottom of the column.
- light boiling components contained in the extraction solvent (A) after use in extractive distillation are extracted with another extraction solvent (B).
- Extraction used in liquid-liquid extraction As the solvent (B), aromatic oil is preferably used.
- Preferred aromatic oils include benzene, toluene or xylene.
- the extraction solvent (A) purified by liquid-liquid extraction is preferably reused in extractive distillation from the viewpoint of economical use of the solvent and reduction of post-treatment cost of the used solvent.
- the most important feature of the present invention is that it is subjected to purification) 3-phenylethyl alcohol is supplied to the rectification column, and) the boiling point difference between 3-phenylethyl alcohol and the off-flavor components produced in the rectification column is utilized, The point is to obtain 3-phenylethyl alcohol (purified as a side cut).
- 3-phenylethyl alcohol is recovered from the top of the rectification column without being according to the present invention, removal of off-flavor components generated in the rectification column becomes insufficient.
- the side cut position can be any position other than the top of the rectification tower, but the separation rate of off-flavor components generated in the rectification tower decreases as it approaches the tower top and increases as it approaches the tower bottom. Therefore, it is advantageous to bring it closer to the tower bottom.
- the side cut position is 5 to 20% of the total number of theoretical plates counted from the top of the rectification column. It is preferable to do.
- the rectifying column a commonly used distillation column such as a perforated plate column, a bubble bell column, or a packed column can be used.
- the operating conditions of the rectification column can usually include a tower top pressure of 0 to 10 1.3 kPa (absolute pressure) and a tower bottom temperature of 100 to 25 Ot :.
- the tower top pressure is preferably 0 to 50 kPa (absolute pressure) and the tower bottom temperature is 150 to 200, More preferably, it is 0.01 to 50 kPa (absolute pressure).
- the fraction obtained from the top of the rectifying column can be subjected to the light boiling separation process helicopter, and the loss of 3-phenylethyl alcohol in the column top component can be suppressed. It is preferable from the viewpoint.
- the recycling position can be any position in the light boiling separation step, but it is preferably an extractive distillation column feed line from the viewpoint of extraction efficiency.
- the 3-phenylethyl alcohol obtained by the present invention is one in which off-flavor components are removed at a particularly high level, and can be optimally used for perfume components.
- Crude ⁇ -phenylethyl alcohol that has passed through the heavy separation process is supplied to the alkaline cleaning tank (5), and at the same time, alkaline water with a caustic soda concentration of 25% by weight is supplied to the alkaline cleaning tank (5). 6 2. It was supplied at a rate of 9 kgZhr.
- the alkaline cleaning tank (5) was operated at a temperature of 80 and atmospheric pressure using a reactor with rotating blades to increase the cleaning efficiency. (Rough after the alkali washing process) 3-phenylethyl alcohol is supplied to the top of the extractive distillation column (9) from the extraction tube (8) at a rate of 30 2.9 kgZhr.
- the number of extraction distillation column (9) was 62, the top pressure was 18.7 kPa, and the reflux ratio was 5.2.
- the light-boiling fraction passes from the top of the extractive distillation column (9) through the extraction tube (1 0) at a rate of 443.9 kgZhr, the liquid-liquid extraction column (1 2) was contacted and mixed with toluene supplied to the bottom of the tower from the supply pipe (13) at a rate of 264.6 kg / hr, and then extracted from the extraction pipe (14).
- the number of stages of the liquid-liquid extraction tower (12) was 100, and the top pressure was 437.8 kPa. Crude i3-phenylethyl alcohol separated from light-boiling components is extracted from the distillation column (9).
- 3_Phenylethyl alcohol (obtained here) has a purity of 99.7% by weight, and the concentrations of phenylacetaldehyde and styrene produced in the rectification column are 43 wt 13111, 0 The weight was 2 ppm, and there was no unpleasant odor and the quality was suitable for use as a fragrance.
- Monophenyl ethyl alcohol was extracted from the top of the rectification column (16) with the operating conditions in each process other than the rectification column (16) being constant.
- the monophenylethyl alcohol obtained here contains phenylacetoaldehyde and styrene produced in the rectification column, 2 12 ppm by weight and 37 ppm by weight, respectively, and has an unpleasant odor. The quality was not suitable for fragrance use.
- the present invention selectively separates and removes off-flavor components generated in the rectification column from / 3-phenylethyl alcohol by simple operation without complicated equipment or operation. It is possible to provide a method for purifying 3-phenylethyl alcohol having a feature of obtaining high-purity 3_phenyl alcohol having an excellent fragrance for a fragrance.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2008800024263A CN101583584B (zh) | 2007-01-18 | 2008-01-17 | β-苯乙醇的纯化方法 |
IL199054A IL199054A (en) | 2007-01-18 | 2009-06-01 | Method of purifying beta-phenylethyl alcohol |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007008886A JP5003172B2 (ja) | 2007-01-18 | 2007-01-18 | β−フェニルエチルアルコールの精製方法 |
JP2007-008886 | 2007-01-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2008088074A1 true WO2008088074A1 (ja) | 2008-07-24 |
Family
ID=39636069
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2008/050925 WO2008088074A1 (ja) | 2007-01-18 | 2008-01-17 | β-フェニルエチルアルコールの精製方法 |
Country Status (4)
Country | Link |
---|---|
JP (1) | JP5003172B2 (ja) |
CN (1) | CN101583584B (ja) |
IL (1) | IL199054A (ja) |
WO (1) | WO2008088074A1 (ja) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104529700A (zh) * | 2014-12-05 | 2015-04-22 | 上海化工研究院 | 一种生物发酵法制备的β-苯乙醇的纯化方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000290205A (ja) * | 1999-04-07 | 2000-10-17 | Sumitomo Chem Co Ltd | β−フェニルエチルアルコールの精製方法 |
JP2000290206A (ja) * | 1999-04-08 | 2000-10-17 | Sumitomo Chem Co Ltd | β−フェニルエチルアルコールの精製方法 |
JP2004182848A (ja) * | 2002-12-03 | 2004-07-02 | Sumitomo Chem Co Ltd | 香料用フェネチルアルコール中のベンジルアルコール含有量の調整方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL190870C (nl) * | 1979-10-16 | 1994-10-03 | Sumitomo Chemical Co | Werkwijze voor het zuiveren van ruwe beta-fenethylalcohol. |
US4400558A (en) * | 1981-04-17 | 1983-08-23 | Atlantic Richfield Company | Recovery of 2-phenylethanol |
SG82692A1 (en) * | 1999-04-07 | 2001-08-21 | Sumitomo Chemical Co | Method for purifying beta-phenylethyl alcohol |
-
2007
- 2007-01-18 JP JP2007008886A patent/JP5003172B2/ja not_active Expired - Fee Related
-
2008
- 2008-01-17 CN CN2008800024263A patent/CN101583584B/zh not_active Expired - Fee Related
- 2008-01-17 WO PCT/JP2008/050925 patent/WO2008088074A1/ja active Application Filing
-
2009
- 2009-06-01 IL IL199054A patent/IL199054A/en not_active IP Right Cessation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000290205A (ja) * | 1999-04-07 | 2000-10-17 | Sumitomo Chem Co Ltd | β−フェニルエチルアルコールの精製方法 |
JP2000290206A (ja) * | 1999-04-08 | 2000-10-17 | Sumitomo Chem Co Ltd | β−フェニルエチルアルコールの精製方法 |
JP2004182848A (ja) * | 2002-12-03 | 2004-07-02 | Sumitomo Chem Co Ltd | 香料用フェネチルアルコール中のベンジルアルコール含有量の調整方法 |
Also Published As
Publication number | Publication date |
---|---|
JP2008174482A (ja) | 2008-07-31 |
CN101583584A (zh) | 2009-11-18 |
JP5003172B2 (ja) | 2012-08-15 |
CN101583584B (zh) | 2013-03-13 |
IL199054A (en) | 2012-06-28 |
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