JP3055248B2 - Method for producing α, β-unsaturated carbonyl compound - Google Patents
Method for producing α, β-unsaturated carbonyl compoundInfo
- Publication number
- JP3055248B2 JP3055248B2 JP3257535A JP25753591A JP3055248B2 JP 3055248 B2 JP3055248 B2 JP 3055248B2 JP 3257535 A JP3257535 A JP 3257535A JP 25753591 A JP25753591 A JP 25753591A JP 3055248 B2 JP3055248 B2 JP 3055248B2
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- producing
- unsaturated carbonyl
- group
- carbonyl compound
- 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 - Fee Related
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Description
【０００１】[0001]
【産業上の利用分野】本発明はプロパルギルアルコール
化合物からα，β−不飽和カルボニル化合物を製造方法
する方法に関する。この方法は各種の農薬、医薬の中間
体等を合成するのに有効な方法である。The present invention relates to a method for producing an α, β-unsaturated carbonyl compound from a propargyl alcohol compound. This method is an effective method for synthesizing various agricultural chemicals, intermediates of pharmaceuticals, and the like.
【０００２】[0002]
【従来の技術】プロパルギルアルコール化合物を転位さ
せてα，β−不飽和カルボニル化合物を製造する方法と
しては、バナジウム、モリブデンまたはタングステンの
オキソ化合物を触媒として用いる方法(Tetrahedron, vo
l.33, pp1775〜1783, 1977) 、チタンと銅または銀をベ
ースにした触媒を用いる方法(Tetrahedron Letters,vo
l.29,No.48,pp6253〜6256,1988)等が知られている。2. Description of the Related Art As a method for producing an α, β-unsaturated carbonyl compound by rearrangement of a propargyl alcohol compound, a method using an oxo compound of vanadium, molybdenum or tungsten as a catalyst (Tetrahedron, Vo.
l.33, pp 1775-1783, 1977), a method using a catalyst based on titanium and copper or silver (Tetrahedron Letters, vo
l.29, No.48, pp6253-6256, 1988).
【０００３】[0003]
【発明が解決しようとする課題】しかしながら、従来公
知の触媒を用いる方法は、高温で行う必要があり、また
ほとんどの方法は二級のプロパルギルアルコール化合物
には適用できず、必ずしも満足できるものではない。However, the method using a conventionally known catalyst needs to be carried out at a high temperature, and most of the methods cannot be applied to secondary propargyl alcohol compounds and are not always satisfactory. .
【０００４】かかる事情に鑑み、本発明者はプロパルギ
ルアルコール化合物を転位させてα，β−不飽和カルボ
ニル化合物を製造する方法について鋭意検討した結果、
過レニウム酸塩およびアリールスルホン酸からなる新触
媒を見出し、本発明を完成するに至った。In view of such circumstances, the present inventors have made intensive studies on a method for producing an α, β-unsaturated carbonyl compound by rearranging a propargyl alcohol compound.
The present inventors have found a new catalyst composed of perrhenate and arylsulfonic acid, and have completed the present invention.
【０００５】[0005]
【課題を解決するための手段】すなわち、本発明は一般
式（１）、 （式中、Ｒ1 は低級アルキル基、フェニル置換アルキル
基またはフェニル基を、Ｒ2 は水素原子または低級アル
キル基を、Ｒ3 は水素原子、フェニル基またはトリメチ
ルシリル基を表す。）で示されるプロパルギルアルコー
ル化合物を過レニウム酸塩およびアリールスルホン酸の
存在下に転位させることを特徴とする一般式（２）、 （式中、Ｒ1 、Ｒ2 およびＲ3 は上記と同じ。）で示さ
れるα，β−不飽和カルボニル化合物の製造方法であ
る。That is, the present invention provides a compound represented by the following general formula (1): (Wherein R 1 represents a lower alkyl group, a phenyl-substituted alkyl group or a phenyl group, R 2 represents a hydrogen atom or a lower alkyl group, and R 3 represents a hydrogen atom, a phenyl group or a trimethylsilyl group). General formula (2), wherein an alcohol compound is rearranged in the presence of a perrhenate and an arylsulfonic acid, (Wherein R 1 , R 2 and R 3 are the same as described above).
【０００６】本発明に用いられるプロパルギルアルコー
ル化合物は二級および三級のプロパルギルアルコール化
合物であり、一般式（１）のＲ1 として具体的にはメチ
ル、エチル、プロピル、ブチル、ペンチル基等の低級ア
ルキル基、２−フェニルエチル、ベンジル基等のフェニ
ル置換アルキル基およびフェニル基が、Ｒ2 として具体
的には水素原子およびメチル、エチル、プロピル、ブチ
ル、ペンチル基等の低級アルキル基が、Ｒ3 として具体
的には水素原子、フェニル基、メチル、エチル、プロピ
ル、ブチル、ペンチル基等の低級アルキル基、トリメチ
ルシリル基が挙げられる。The propargyl alcohol compound used in the present invention is a secondary or tertiary propargyl alcohol compound. Specific examples of R 1 in the general formula (1) include lower groups such as methyl, ethyl, propyl, butyl and pentyl groups. alkyl group, 2-phenylethyl, phenyl-substituted alkyl group and a phenyl group or a benzyl group, specifically a hydrogen atom and methyl as R 2, ethyl, propyl, butyl, lower alkyl groups such as pentyl, R 3 Specific examples include a hydrogen atom, a phenyl group, a lower alkyl group such as methyl, ethyl, propyl, butyl, and pentyl group, and a trimethylsilyl group.
【０００７】プロパルギルアルコール化合物としてさら
に具体的には、１−フェニル−プロパン−２−イン−１
−オール、１−フェニル−ヘプタン−２−イン−１−オ
ール、１−フェニル−３−トリメチルシリル−ヘプタン
−２−イン−１−オール、１−フェニル−３−メチル−
ペンタン−４−イン−３−オール、１−フェニル−３−
メチル−ノナン−４−イン−３−オール、７−フェニル
−ヘプタン−６−イン−５−オール等が挙げられる。More specifically, the propargyl alcohol compound is 1-phenyl-propan-2-yne-1
-Ol, 1-phenyl-heptane-2-yn-1-ol, 1-phenyl-3-trimethylsilyl-heptane-2-yn-1-ol, 1-phenyl-3-methyl-
Pentan-4-yn-3-ol, 1-phenyl-3-
Methyl-nonane-4-yn-3-ol, 7-phenyl-heptane-6-yn-5-ol, and the like.
【０００８】本発明に用いられる過レニウム酸塩として
は、過レニウム酸テトラアンモニウム、過レニウム酸テ
トラメチルアンモニウム、過レニウム酸テトラエチルア
ンモニウム、過レニウム酸テトラプロピルアンモニウ
ム、過レニウム酸テトラブチルアンモニウム、過レニウ
ム酸テトラペンチルアンモニウム等が挙げられる。The perrhenate used in the present invention includes tetraammonium perrhenate, tetramethylammonium perrhenate, tetraethylammonium perrhenate, tetrapropylammonium perrhenate, tetrabutylammonium perrhenate, perrhenium And tetrapentyl ammonium acid.
【０００９】本発明に用いられるアリールスルホン酸と
しては、ベンゼンスルホン酸、パラトルエンスルホン酸
およびメタニトロベンゼンスルホン酸等が挙げられる。The arylsulfonic acid used in the present invention includes benzenesulfonic acid, p-toluenesulfonic acid, and metanitrobenzenesulfonic acid.
【００１０】本発明は通常、溶媒の存在下に行われる。
溶媒は特に限定されるものではないが、ジクロルメタ
ン、１，２−ジクロルエタン、１，１，２−トリクロル
エタンおよびクロロホルム等の塩素化炭化水素が好まし
く用いられる。[0010] The present invention is generally carried out in the presence of a solvent.
The solvent is not particularly limited, but chlorinated hydrocarbons such as dichloromethane, 1,2-dichloroethane, 1,1,2-trichloroethane and chloroform are preferably used.
【００１１】反応は通常、プロパルギルアルコール化合
物を溶解したジクロルメタン溶液と過レニウム酸塩とア
リールスルホン酸のジクロルメタン溶液とを混合し、常
温または必要により加熱し、攪拌して行われる。The reaction is usually carried out by mixing a dichloromethane solution in which a propargyl alcohol compound is dissolved, and a dichloromethane solution of a perrhenate salt and an arylsulfonic acid, and heating at room temperature or, if necessary, with stirring.
【００１２】[0012]
【発明の効果】本発明の方法によれば、低温でプロパル
ギルアルコール化合物を転位させて、α，β−不飽和カ
ルボニル化合物を収率良く製造することができる。本発
明は二級のプロパルギルアルコール化合物に適用するこ
とができ、その意義は大きい。According to the method of the present invention, an α, β-unsaturated carbonyl compound can be produced in good yield by rearranging a propargyl alcohol compound at a low temperature. The present invention can be applied to a secondary propargyl alcohol compound, and its significance is great.
【００１３】[0013]
【実施例】以下、本発明を実施例でさらに詳細に説明す
るが、本発明はこれらの実施例に限定されるものではな
い。EXAMPLES Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited to these Examples.
【００１４】実施例１ １−フェニル−プロパン−２−イン−１−オール（４
３．５ｍｇ，０．３３ｍｍｏｌ）のジクロルメタン（２
ｍｌ）溶液と、過レニウム酸テトラブチルアンモニウム
（Inorganic Synthesis 26,391(1989)に記載の方法によ
り合成した。）（１６．６ｍｇ，０．０３３ｍｍｏｌ）
とパラトルエンスルホン酸一水和物（６．６ｍｇ，０．
０３３ｍｍｏｌ）のジクロルメタン（１．５ｍｌ）溶液
を混合し、室温で２時間攪拌して転位反応を行った。Example 1 1-phenyl-propan-2-yn-1-ol (4
3.5 mg, 0.33 mmol) of dichloromethane (2
ml) solution and tetrabutylammonium perrhenate (synthesized by the method described in Inorganic Synthesis 26,391 (1989)) (16.6 mg, 0.033 mmol).
And paratoluenesulfonic acid monohydrate (6.6 mg, 0.1 g).
033 mmol) in dichloromethane (1.5 ml) was mixed and stirred at room temperature for 2 hours to carry out a rearrangement reaction.
【００１５】反応液に飽和炭酸水素ナトリウム溶液とジ
エチルエーテルを加えて攪拌した。有機層を塩水で洗
い、無水硫酸ナトリウムで乾燥した。次いで溶媒のジク
ロルメタンを真空に引いて除き、得られた粗生成物を薄
層クロマトグラフ（シリカゲル、展開液はヘキサンと酢
酸エチルが５：１の溶液）で転位生成物を分離した。転
位生成物である１−フェニル−１−エテン−２−アール
が４０．１ｍｇ（０．３０ｍｍｏｌ）生成していた。収
率は９２％である。[0015] A saturated sodium hydrogen carbonate solution and diethyl ether were added to the reaction solution, and the mixture was stirred. The organic layer was washed with brine and dried over anhydrous sodium sulfate. Then, the solvent, dichloromethane, was removed by vacuum, and the resulting crude product was separated by thin-layer chromatography (silica gel, developing solution of hexane and ethyl acetate in a 5: 1 solution) to separate the rearranged product. 40.1 mg (0.30 mmol) of 1-phenyl-1-ethene-2-al as a rearrangement product was produced. The yield is 92%.
【００１６】実施例２〜８、比較例１ Ｒ1 、Ｒ2 、Ｒ3 が表１に示すプロパルギルアルコール
化合物について実施例１と同様に反応分離を行った。実
施例７、８については溶媒の還流下に反応を行った。結
果を表１に示す。Examples 2 to 8 and Comparative Example 1 Propargyl alcohol compounds having R 1 , R 2 and R 3 shown in Table 1 were subjected to reaction separation in the same manner as in Example 1. In Examples 7 and 8, the reaction was carried out under reflux of the solvent. Table 1 shows the results.
【００１７】[0017]
【表１】 [Table 1]
フロントページの続き (51)Int.Cl.7 識別記号 ＦＩ Ｃ０７Ｃ 49/794 Ｃ０７Ｃ 49/794 Ｃ０７Ｆ 7/08 Ｃ０７Ｆ 7/08 Ａ // Ｃ０７Ｂ 61/00 ３００ Ｃ０７Ｂ 61/00 ３００ (56)参考文献 特開 昭51−48608（ＪＰ，Ａ) 特開 昭55−153735（ＪＰ，Ａ) 特開 昭60−34926（ＪＰ，Ａ) 特開 昭55−27135（ＪＰ，Ａ) 特開 昭60−45544（ＪＰ，Ａ) 特開 昭47−42709（ＪＰ，Ａ) 特開 昭57−116024（ＪＰ，Ａ) (58)調査した分野(Int.Cl.7，ＤＢ名) C07C 45/51 C07C 47/21 C07C 47/232 C07C 49/794 C07C 49/203 C07C 45/54 C07F 7/08 C07B 61/00 300 Continued on the front page (51) Int.Cl. 7 Identification symbol FI C07C 49/794 C07C 49/794 C07F 7/08 C07F 7/08 A // C07B 61/00 300 C07B 61/00 300 (56) References Special JP-A-51-48608 (JP, A) JP-A-55-153735 (JP, A) JP-A-60-34926 (JP, A) JP-A-55-27135 (JP, A) JP-A-60-45544 (JP, A) JP, A) JP-A-47-42709 (JP, A) JP-A-57-116024 (JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) C07C 45/51 C07C 47/21 C07C 47/232 C07C 49/794 C07C 49/203 C07C 45/54 C07F 7/08 C07B 61/00 300
Claims (1)
基またはフェニル基を、Ｒ2 は水素原子または低級アル
キル基を、Ｒ3 は水素原子、フェニル基またはトリメチ
ルシリル基を表す．）で示されるプロパルギルアルコー
ル化合物を過レニウム酸塩およびアリールスルホン酸の
存在下に転位させることを特徴とする一般式（２）、 （式中、Ｒ1 、Ｒ2 およびＲ3 は上記と同じ。）で示さ
れるα，β−不飽和カルボニル化合物の製造方法。(1) a general formula (1), Wherein R 1 represents a lower alkyl group, a phenyl-substituted alkyl group or a phenyl group, R 2 represents a hydrogen atom or a lower alkyl group, and R 3 represents a hydrogen atom, a phenyl group or a trimethylsilyl group. General formula (2), wherein an alcohol compound is rearranged in the presence of a perrhenate and an arylsulfonic acid, (In the formula, R 1 , R 2 and R 3 are the same as above.) A method for producing an α, β-unsaturated carbonyl compound represented by the formula:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3257535A JP3055248B2 (en) | 1991-10-04 | 1991-10-04 | Method for producing α, β-unsaturated carbonyl compound |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3257535A JP3055248B2 (en) | 1991-10-04 | 1991-10-04 | Method for producing α, β-unsaturated carbonyl compound |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0597758A JPH0597758A (en) | 1993-04-20 |
| JP3055248B2 true JP3055248B2 (en) | 2000-06-26 |
Family
ID=17307638
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3257535A Expired - Fee Related JP3055248B2 (en) | 1991-10-04 | 1991-10-04 | Method for producing α, β-unsaturated carbonyl compound |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3055248B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101529337B1 (en) * | 2007-05-16 | 2015-06-16 | 바스프 에스이 | Method for producing vinyl esters of carboxylic acids |
| JP5172249B2 (en) * | 2007-09-04 | 2013-03-27 | 静岡県公立大学法人 | Composite metal catalyst |
-
1991
- 1991-10-04 JP JP3257535A patent/JP3055248B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0597758A (en) | 1993-04-20 |
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