Formaldehyde → Dihydrobenzoxazine

HRID 1928517

反応式

HRID 1928517 の反応式
[NH2:1][CH2:2][C:3]12CCCC1C1CC2(CN)CC1.[C:15]1([OH:21])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.C=O>C(Cl)(Cl)Cl>[O:21]1[C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[CH2:3][CH2:2][NH:1]1

参加物

5

反応物 3

HCID 712FormaldehydeHCID 996Phenol2 回HCID 53737527Bis(aminomethyl)tricyclo[5,2,1,02,6]decane

生成物 1

HCID 21887592Dihydrobenzoxazine

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒2 回

反応条件

温度
60 °C

実験手順

One mole of 3(4),8(9),-bis(aminomethyl)tricyclo[5,2,1,02,6]decane as saturated alicyclic hydrocarbon diamine compound having a condensed ring structure, two moles of phenol as the phenol compound represented by Formula (1), as well as, 4 moles of paraformaldehyde as aldehyde compound and 1500 g of chloroform were mixed. This mixture was heated to 60° C. under stirring, and the reaction was carried out for 6 hours since chloroform started circulating. After the end of the reaction, the reaction mixture was washed with an aqueous solution of 1 N sodium hydroxide, and then rinsed with ion exchanged water. Then, after the chloroform phase was dried with anhydrous sodium sulfate, chloroform was evaporated with a rotary evaporator to obtain a bifunctional dihydro benzoxazine compound in which R14 of Formula (2) is the amino residue of 3(4),8(9),-bis(aminomethyl)tricyclo[5,2,1,02,6]decane.

後処理

  1. customAfter the end of the reaction
  2. washthe reaction mixture was washed with an aqueous solution of 1 N sodium hydroxide
  3. washrinsed with ion
  4. dry with materialThen, after the chloroform phase was dried with anhydrous sodium sulfate, chloroform
  5. customwas evaporated with a rotary evaporator

出典と根拠

ORDレコード
ord-0c98b5027cee4fd08448c6f83a4a0314
出典データセット
uspto-grants-2012_05
特許番号
US08183368B2

関連ノート

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