JP2005255587A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2005255587A5 JP2005255587A5 JP2004067373A JP2004067373A JP2005255587A5 JP 2005255587 A5 JP2005255587 A5 JP 2005255587A5 JP 2004067373 A JP2004067373 A JP 2004067373A JP 2004067373 A JP2004067373 A JP 2004067373A JP 2005255587 A5 JP2005255587 A5 JP 2005255587A5
- Authority
- JP
- Japan
- Prior art keywords
- meth
- acrylic acid
- cyclic skeleton
- washing
- amines
- 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.)
- Granted
Links
Description
本発明は、炭素数4以上の環式骨格を有するアルコール(以下、これを環式骨格含有アルコールと略称する)と(メタ)アクリル酸またはその反応性誘導体を反応させる工程、および該工程で得られる反応生成物を、アンモニアまたはアミン類を含む洗浄液で洗浄する工程を含むことを特徴とする環式骨格含有(メタ)アクリル酸エステルの製造方法である。 The present invention provides a process of reacting an alcohol having a cyclic skeleton having 4 or more carbon atoms (hereinafter abbreviated as a cyclic skeleton-containing alcohol) with (meth) acrylic acid or a reactive derivative thereof, and the process. The reaction product obtained is a method for producing a cyclic skeleton-containing (meth) acrylic acid ester comprising a step of washing with a washing liquid containing ammonia or amines.
次に、環式骨格含有アルコールと(メタ)アクリル酸またはその反応性誘導体との反応生成物の洗浄工程について説明する。
上記の工程で得られる反応生成物(反応混合物)は、アンモニアまたはアミン類を含む水溶液(洗浄液)で洗浄する。かかるアミン類としては、(メタ)アクリル酸またはその反応性誘導体や触媒、(メタ)アクリル酸由来のオリゴマーなどと反応して水溶性の化合物を与えるアミン類であればよく、例えばメチルアミン、エチルアミン、プロピルアミン、ブチルアミン、ジメチルアミン、ジエチルアミン、トリメチルアミン、トリエチルアミン、ピリジンなどを使用することができる。操作性を考慮すれば、洗浄液としては、アンモニア水、トリエチルアミンを含む水溶液を使用するのが好ましい。洗浄液中のアンモニアまたはアミン類の濃度は、1〜25重量%の範囲であるのが好ましく、1〜10重量%の範囲であるのがより好ましい。この洗浄処理により、反応混合物中に含まれる未反応原料[環式骨格含有アルコール、(メタ)アクリル酸またはその反応性誘導体]や触媒、(メタ)アクリル酸由来のオリゴマー、その他の水溶性不純物が効率よく除去される。
Next, the washing | cleaning process of the reaction product of cyclic skeleton containing alcohol and (meth) acrylic acid or its reactive derivative is demonstrated.
The reaction product (reaction mixture) obtained in the above step is washed with an aqueous solution (washing solution) containing ammonia or amines. Such amines, (meth) acrylic acid or a reactive derivative thereof and the catalyst may be a amine to give (meth) compounds such as reacting with the water-soluble oligomer derived from an acrylic acid, For example main ethylamine, Ethylamine, propylamine, butylamine, dimethylamine, diethylamine, trimethylamine, triethylamine, pyridine and the like can be used . Considering operability, as the cleaning liquid, aqueous ammonia is preferable to use an aqueous solution containing triethylamine. The concentration of ammonia or amines in the cleaning liquid is preferably in the range of 1 to 25% by weight, more preferably in the range of 1 to 10% by weight. By this washing treatment, unreacted raw material [cyclic skeleton-containing alcohol, (meth) acrylic acid or a reactive derivative thereof], catalyst, oligomer derived from (meth) acrylic acid, and other water-soluble impurities contained in the reaction mixture. It is efficiently removed.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004067373A JP4545459B2 (en) | 2004-03-10 | 2004-03-10 | Method for producing cyclic skeleton-containing (meth) acrylic acid ester |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004067373A JP4545459B2 (en) | 2004-03-10 | 2004-03-10 | Method for producing cyclic skeleton-containing (meth) acrylic acid ester |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2005255587A JP2005255587A (en) | 2005-09-22 |
JP2005255587A5 true JP2005255587A5 (en) | 2006-10-12 |
JP4545459B2 JP4545459B2 (en) | 2010-09-15 |
Family
ID=35081675
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2004067373A Expired - Fee Related JP4545459B2 (en) | 2004-03-10 | 2004-03-10 | Method for producing cyclic skeleton-containing (meth) acrylic acid ester |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP4545459B2 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005255586A (en) * | 2004-03-10 | 2005-09-22 | Kuraray Co Ltd | Method for producing lactone skeleton-containing (meth)acrylic acid ester |
JP2005255584A (en) * | 2004-03-10 | 2005-09-22 | Kuraray Co Ltd | Method for producing lactone skeleton-containing (meth)acrylic acid ester |
JP2005255583A (en) * | 2004-03-10 | 2005-09-22 | Kuraray Co Ltd | Method for producing cyclic skeleton-containing (meth)acrylic acid ester |
JP4827168B2 (en) * | 2005-09-29 | 2011-11-30 | 三菱レイヨン株式会社 | Method for producing (meth) acrylic acid ester |
JP5008311B2 (en) * | 2006-02-08 | 2012-08-22 | 大阪有機化学工業株式会社 | Method for producing six-membered lactone (meth) acrylic acid ester |
JP5175460B2 (en) * | 2006-08-24 | 2013-04-03 | 出光興産株式会社 | Process for producing (meth) acrylic acid oxoadamantyl esters |
JP2014205662A (en) * | 2013-03-19 | 2014-10-30 | 三菱レイヨン株式会社 | Production method of (meth)acrylate |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63275544A (en) * | 1987-05-06 | 1988-11-14 | Osaka Yuki Kagaku Kogyo Kk | Stabilization of ester |
JP2001192356A (en) * | 1999-10-27 | 2001-07-17 | Daicel Chem Ind Ltd | Method for producing (meth)acrylic acid ester having cyclic skeleton |
JP5064614B2 (en) * | 2001-02-01 | 2012-10-31 | 株式会社ダイセル | Method for producing (meth) acrylic acid ester having cyclic skeleton |
-
2004
- 2004-03-10 JP JP2004067373A patent/JP4545459B2/en not_active Expired - Fee Related
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2005255587A5 (en) | ||
JPS61275241A (en) | Production of deuterated acrylic acid or methacrylic acid | |
CN107308883B (en) | A kind of stable foam formed by abietyl amino acid surfactant | |
JP2004532319A5 (en) | ||
WO1994014737A1 (en) | Process for producing 1,1,2,2,3-pentafluoropropane | |
JP2012500273A (en) | Process for the production of N-alkyl (alkyl) acrylamides | |
JP2006523225A5 (en) | ||
JP3553335B2 (en) | Method for producing high quality tertiary amine | |
CN108863836A (en) | A kind of abietyl grape sugar surfactant and its application | |
CN100358858C (en) | Method for preparing lefluthrin | |
JP3554924B2 (en) | Method for producing free hydroxylamine aqueous solution | |
JP3646328B2 (en) | Treatment method of ethylenediamine-containing waste liquid | |
JP2002285469A5 (en) | ||
JPS6330450A (en) | Production of deuterated benzoic acid | |
JP2005255586A5 (en) | ||
Bianco et al. | Design and synthesis of a new furanosic sialylmimetic as a potential influenza neuraminidase viral inhibitor | |
CN103421037B (en) | The synthesis technique of 1-ethoxycarbonyl-5-methyl-(3R)-tertiary butyl dimethylsilyloxy glutarate | |
JP2793281B2 (en) | Method for producing amine oxide | |
Rivera et al. | An Expeditious Synthesis Of 3-Amino B-Lactams Derived From Polyaromatic Compounds | |
JPH0977725A (en) | Production of lysine salt of fatty acid | |
JP2011153099A (en) | Method for producing (e)-2-hexenyl=(e)-2-hexenoate | |
RU2414452C1 (en) | Method for simultaneous production of 2-nitro-5-chloroaniline and 2-nitro-4-chloroaniline | |
CN102553551B (en) | Oligopeptide-like chiral selector and preparation method thereof | |
JPH02104560A (en) | Production of optically active 2-chloropropionic acid ester | |
JP5209201B2 (en) | Method for producing high-purity organic acid chloride having an unsaturated group in the molecule |