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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Water → Mono-methoxy diethylene glycol monoacrylate

HRID 5203
ノート
印刷プレビュー

反応式

HRID 5203 の反応式
[CH3:1][O:2][CH2:3][CH2:4][O:5][CH2:6][CH2:7][OH:8].[C:9]([OH:13])(=[O:12])[CH:10]=[CH2:11].C1(C)C=CC(S(O)(=O)=[O:21])=CC=1.O>C1(C)C=CC=CC=1>[C:9]([OH:13])(=[O:12])[CH:10]=[CH2:11].[CH3:1][O:2][CH:3]([OH:21])[CH2:4][O:5][CH2:6][CH2:7][OH:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 6101p-Toluenesulfonic acidHCID 6581Acrylic AcidHCID 8134Diethylene Glycol Monomethyl Ether

生成物 1

HCID 87063345Mono-methoxy diethylene glycol monoacrylate

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

682 grams Methyl Carbitol (diethylene glycol monomethyl ether, Union Carbide) were azeotropically esterified with 598.9 grams acrylic acid in 272 grams toluene in the presence of 22.8 grams p-toluenesulfonic acid and inhibitors until no more water was collected. Conditions were 95°-98° C., nitrogen sparge in vacuo. On completion, the product was washed and neutralized with sodium carbonate. 1,300 ppm p-methoxyphenol were added and solvent removed at 80° C. at maximum vacuum with an air sparge. Filter aid was added and the product filtered to clarity at 50° C. The final product was a clear, light yellow liquid, viscosity 6 cps with a Gardner 1 color.

後処理

  1. customwas collected
  2. customwere 95°-98° C.
  3. customnitrogen sparge in vacuo
  4. washOn completion, the product was washed
  5. addition1,300 ppm p-methoxyphenol were added
  6. customsolvent removed at 80° C. at maximum vacuum with an air
  7. customsparge
  8. filtrationFilter aid
  9. additionwas added
  10. filtrationthe product filtered to clarity at 50° C

出典と根拠

ORDレコード
ord-0490a3c74fb84af38fee37a9f0e79743
出典データセット
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05243085

反応ノート

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