JPS58180557A - Fluoran derivative - Google Patents

Fluoran derivative

Info

Publication number
JPS58180557A
JPS58180557A JP6507682A JP6507682A JPS58180557A JP S58180557 A JPS58180557 A JP S58180557A JP 6507682 A JP6507682 A JP 6507682A JP 6507682 A JP6507682 A JP 6507682A JP S58180557 A JPS58180557 A JP S58180557A
Authority
JP
Japan
Prior art keywords
formula
sensitive recording
recording paper
heat
crystals
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.)
Pending
Application number
JP6507682A
Other languages
Japanese (ja)
Inventor
Hiroshi Goto
寛 後藤
Shigeru Higeta
茂 日下田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ricoh Co Ltd
Original Assignee
Ricoh Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Ricoh Co Ltd filed Critical Ricoh Co Ltd
Priority to JP6507682A priority Critical patent/JPS58180557A/en
Publication of JPS58180557A publication Critical patent/JPS58180557A/en
Pending legal-status Critical Current

Links

Abstract

NEW MATERIAL:A fluoran derivative of formula I . USE:A coloring component in heat-sensitive recording materials; a color forming dye in recording paper such as press.-sensitive recording paper or conducting heat-sensitive recording paper. PREPARATION:5-Methyl-4-N-ethylamino-2-hydroxy-2'-carboxybenzophenone of formula II is reacted with 4-methoxy-2'-chlorodiphenylamine of formula III at -10-100 deg.C for several to tens of hr using a condensing agent such as sulfuric acid or polyphosphoric acid. The reaction product is poured into ice water and the deposited crystals are separated from the soln. by filtration. Then, the obtained crystals are dispersed in a 1-20% aq. sodium hydroxide soln. with stirring at 0-100 deg.C for several hr. The crystals are then filtered, dried, and recrystalized from an org. solvent such as toluene, benzene, or isopropyl alc. to yield a fluoran derivative of formula I .

Description

【発明の詳細な説明】 本発明は、式(I) で表わされる新規フルオラン誘導体及びこれを感熱発色
成分として用いる感熱記録材料に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel fluoran derivative represented by formula (I) and a heat-sensitive recording material using the same as a heat-sensitive coloring component.

一般に、フルオラン誘導体は、感熱記録材料における発
色成分として用゛いられており、その他感圧記録紙、通
電記録紙などの記録紙における発色性色素としても利用
されている。このようなフルオラン系色素の中、例えば
、赤色発色用としては、3−ジエチルアミノ−6−メチ
ル−7−クロロフルオラン(mp=235 C)など広
く利用されてきた。
Fluorane derivatives are generally used as color-forming components in heat-sensitive recording materials, and are also used as color-forming dyes in recording papers such as pressure-sensitive recording paper and current-carrying recording paper. Among such fluoran dyes, for example, 3-diethylamino-6-methyl-7-chlorofluoran (mp=235 C) has been widely used for red coloring.

しかしながら、このようなフルオラン誘導体は、その融
点が200C以上と高いために、感熱記録7−トとした
場合に、熱感度の良好なものを得ることは困難であった
。殊に、前記した従来一般に適用されている赤色発色用
のフルオラン誘導体を用いた感熱記録シートは安定性が
悪く、長時間の光照射により地肌部が赤く着色して地肌
カブリを生じたり、赤色画像が退色してしまうなどの欠
点を有している。
However, since such fluorane derivatives have a high melting point of 200 C or more, it has been difficult to obtain a material with good thermal sensitivity when used as a thermal recording medium. In particular, the heat-sensitive recording sheets using fluorane derivatives for red coloring, which have been commonly applied in the past, have poor stability, and when exposed to light for a long period of time, the background becomes red, causing background fog, and red images are It has disadvantages such as discoloration.

本発明による前記式(I)で表わされるフルオラン誘導
体は、それ自体は殆んど無色の物質であるが、ビスフU
−ルAなどの電子受容性物質と緊密に接触させることに
より赤色に発色する性質を有し、しかもその融点は18
5〜186.5 Cであり、熱感度においてもすぐれて
いる。さらに、このフルオラン誘導体を用いて形成した
感熱記録シートは、安定性がよく、保存中に着色を生ず
ることがない一ト発色画像が退色したり、地肌部に著し
いカブリが生じるようなことはない。
The fluoran derivative represented by the formula (I) according to the present invention is an almost colorless substance itself, but
- It has the property of developing a red color when brought into close contact with an electron-accepting substance such as Lure A, and its melting point is 18
5 to 186.5 C, and has excellent thermal sensitivity. Furthermore, the heat-sensitive recording sheet formed using this fluoran derivative has good stability and does not cause coloring during storage, does not cause color fading of the one-tone image, and does not cause significant fogging on the background. .

本発明のフルオラン誘導体を合成するには、下記反応式
で示すように、式(1)の5−メチル−4−N−エチル
アミノ−2−ヒドロキシ−2′−カルボキシベンゾフェ
ノンと式(1111の4−メトキ/−2’−クロロ7フ
ーエニルアミンとを、硫酸、ポIJ IJン酸などの脱
水縮合剤を用いて一10C〜100Cの温度で数時間〜
数十時間反応させる。次いで、反応物を氷水中に注加し
、析出物を濾過し、この結晶を1〜20チの苛性ソーダ
水溶液中に分散し、0〜100Cで数時間攪拌する。次
いで結晶を濾過シ、乾燥後トルエン、ベンセン、インプ
ロピルアルコールなどの有機溶剤で再結晶することによ
り式(11で示されるフルオラン誘導体を得ることがで
きる。
To synthesize the fluoran derivative of the present invention, as shown in the reaction formula below, 5-methyl-4-N-ethylamino-2-hydroxy-2'-carboxybenzophenone of formula (1) and 4 of formula (1111) are synthesized. -methoxy/-2'-chloro7-phenylamine using a dehydration condensation agent such as sulfuric acid or polyhydric acid at a temperature of -10C to 100C for several hours.
Let it react for several tens of hours. Next, the reactant is poured into ice water, the precipitate is filtered, and the crystals are dispersed in 1 to 20 g of aqueous sodium hydroxide solution and stirred at 0 to 100 C for several hours. The crystals are then filtered, dried, and then recrystallized with an organic solvent such as toluene, benzene, or inpropyl alcohol to obtain a fluoran derivative represented by formula (11).

本発明のフルオラン誘導体を用いた感熱記録ノートは、
従来公知の方法に従って製造することができる。即ち本
発明によるフルオラン誘導体とフェノール性化合物やそ
の他の電子受容性物質とを・・インダーを用いて紙、プ
ラスチックフィルム、布などの支持体に対して一層又は
多層状に塗布乾燥して支持させればよい。さらに塗布層
中には、増白効果や筆記性を向上させるためにCaC0
a 。
The heat-sensitive recording notebook using the fluorane derivative of the present invention is
It can be manufactured according to a conventionally known method. That is, the fluoran derivative according to the present invention and a phenolic compound or other electron-accepting substance are coated in a single layer or in multiple layers on a support such as paper, plastic film, cloth, etc. using an inder and then dried and supported. Bye. Furthermore, in the coating layer, CaC0 is added to improve the whitening effect and writability.
a.

TiO2、ZnO、タルク、クレイ、カオリン等の無機
填料及びその他の有機填料さらにこの種感熱記録シート
に慣用されている任意の補助添加成分を加えることかで
きる。
Inorganic fillers such as TiO2, ZnO, talc, clay, kaolin, and other organic fillers, as well as any auxiliary additive components commonly used in this type of heat-sensitive recording sheet, may be added.

次に本発明を合成例又は実施例によりさらに詳細に説明
する。
Next, the present invention will be explained in more detail with reference to Synthesis Examples or Examples.

合成例1 (2−メチル−3−N−エチルアミノ−7−〇−クロロ
アニリノフルオランの合成) 5−メチル−1l−N−エチルアミノ−2−ヒドロキノ
−2′−カルボキシベンゾフエノン7、18 Pと4−
メトキシ−2′−クロロジフェニルアミン4671を9
5%硫酸5Q+++ff中に溶解し、室温で約50時間
攪拌する。反応終了後反応液を氷水500m1中に注加
し、析出物を濾過する。次いでこの結晶を5%苛性ソー
ダ水溶液中に乾燥後トルエンで再結晶を行ない、殆んど
白色の結晶491を得た。mp 185〜186.5 
U元素分析結果帳) 水素 炭素 窒素 計算値 4.81 72,11 5.80実測値 4.
77 72,18 5.76本合成例で得られた化合物
とビスフェノールAとの発色色相は濃赤色で、シリカゲ
ル上でも赤色を示す。
Synthesis Example 1 (Synthesis of 2-methyl-3-N-ethylamino-7-〇-chloroanilinofluorane) 5-Methyl-1l-N-ethylamino-2-hydroquino-2'-carboxybenzophenone 7 , 18 P and 4-
Methoxy-2'-chlorodiphenylamine 4671 9
Dissolve in 5% sulfuric acid 5Q+++ff and stir at room temperature for about 50 hours. After the reaction is completed, the reaction solution is poured into 500 ml of ice water, and the precipitate is filtered. Next, the crystals were dried in a 5% aqueous sodium hydroxide solution and recrystallized with toluene to obtain almost white crystals 491. mp 185-186.5
U elemental analysis result book) Hydrogen Carbon Nitrogen Calculated value 4.81 72,11 5.80 Actual value 4.
77 72,18 5.76 The coloring hue of the compound obtained in this synthesis example and bisphenol A is deep red, and it also shows red on silica gel.

実施例I A液: 水                       1
51B液: 水                       1
5グ各液を磁性ボールミル中で2日間分散した後、A液
及びB液を1:3(重量比)の割合で混合し、これに酸
化殿粉の20係水溶液を乾燥重量比が下記のように添加
混合して感熱層用塗布液とする。
Example I Liquid A: Water 1
51B liquid: 1 water
After dispersing each of the 5g liquids in a magnetic ball mill for 2 days, liquids A and B were mixed at a ratio of 1:3 (weight ratio), and a 20% aqueous solution of oxidized starch was added to this in a dry weight ratio as follows: A coating solution for a heat-sensitive layer is prepared by adding and mixing the components as follows.

素         材     乾燥重量比2−メチ
ル−3−N−エチルアミノ− 7−0−クロロアニリノフルオラン    1酸化殿粉
             16次に、この塗布液を基
準秤量52 ?/nXの上質紙の片面に乾燥付着量4 
El/m’になるようワイヤー・・−で塗布し、感熱記
録紙サンプルAを得た。
Materials Dry weight ratio 2-Methyl-3-N-ethylamino-7-0-chloroanilinofluorane monoxide starch 16 Next, the standard weight of this coating solution was 52? Dry adhesion amount 4 on one side of /nX high-quality paper
A thermal recording paper sample A was obtained by coating with a wire so as to achieve El/m'.

比較例1 A液における2−メチル−3−エチルアミノ−7−0−
クロロアニリノフルオランの代りに3−ジエチルアミン
−6−メチル−7−クロロフルオランを用いた以外は同
様にして感熱記録紙サンプルBを得た。
Comparative Example 1 2-Methyl-3-ethylamino-7-0- in Solution A
A thermal recording paper sample B was obtained in the same manner except that 3-diethylamine-6-methyl-7-chlorofluoran was used instead of chloroanilinofluoran.

前記のようにして得たそれぞれの感熱記録紙をファクシ
ミリ装置(RIFA、X−303)で印字(印字電圧1
3.08V)したところ本発明によるサンプルAは濃い
赤色を示し、またその画像濃度は093を示したのに対
し、比較のためのサンプルBは赤色を示し、またその画
像濃度は0.89を示した。
Each heat-sensitive recording paper obtained as described above is printed using a facsimile machine (RIFA, X-303) (printing voltage 1
3.08V) Sample A according to the present invention showed a deep red color and an image density of 0.93, whereas sample B for comparison showed a red color and an image density of 0.89. Indicated.

さらに、実施例1と比較例1で得られた両方の感熱記録
紙を40C1湿度95%RHで24時間放置した際の地
肌の変色濃度をみた。濃度はマクベス濃度計で黄色フィ
ルターを使って測定した。
Furthermore, the discoloration density of the background was observed when both the thermosensitive recording papers obtained in Example 1 and Comparative Example 1 were left at 40C1 humidity 95% RH for 24 hours. Concentrations were measured using a Macbeth densitometer using a yellow filter.

実施例1の感熱記録紙の地肌部濃度は、OO8であった
が、比較例1では0.12と地肌の着色が大きかった。
The background density of the thermal recording paper of Example 1 was OO8, but in Comparative Example 1, the density was 0.12, which was large in coloring of the background.

本発明新規フルオラン誘導体は熱感度、画像濃度に著し
く優れ、さらに地肌カブリが少なく保存性もよい感熱記
録シートを提供した。
The novel fluorane derivative of the present invention provided a heat-sensitive recording sheet which was extremely excellent in thermal sensitivity and image density, and further had less background fog and good storage stability.

代理人 弁理士池浦敏明Agent: Patent attorney Toshiaki Ikeura

Claims (2)

【特許請求の範囲】[Claims] (1)式 で表わされるフルオラン誘導体。(1) Formula A fluoran derivative represented by (2)式 で表わされるフルオラン誘導体を感熱発色成分として用
いることを特徴とする感熱記録材料。
A heat-sensitive recording material characterized in that a fluoran derivative represented by the formula (2) is used as a heat-sensitive coloring component.
JP6507682A 1982-04-19 1982-04-19 Fluoran derivative Pending JPS58180557A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6507682A JPS58180557A (en) 1982-04-19 1982-04-19 Fluoran derivative

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6507682A JPS58180557A (en) 1982-04-19 1982-04-19 Fluoran derivative

Publications (1)

Publication Number Publication Date
JPS58180557A true JPS58180557A (en) 1983-10-22

Family

ID=13276494

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6507682A Pending JPS58180557A (en) 1982-04-19 1982-04-19 Fluoran derivative

Country Status (1)

Country Link
JP (1) JPS58180557A (en)

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