HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277485Generated: October 25, 2026
Water → 2-phthalimido-N-(1,1,5-trimethylhexyl)acetamide
https://huagongshe.com/reaction/1277485
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2,6-Dimethyl-2-heptanol | HCID 83268 | — |
| Reactant | N-(Cyanomethyl)-phthalimide | HCID 345881 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-phthalimido-N-(1,1,5-trimethylhexyl)acetamide | HCID 23454150 | — |
Reaction Steps
A suspension of phthalimidoacetonitrile (6.01 g, 0.03 mole) in glacial acetic acid (16 ml) was heated to 60° C. with stirring; 2,6-dimethylheptan-2-ol (4.64 g, 0.03 mole) was then added followed dropwise by concentrated sulphuric acid (4.4 ml, 0.08 mole). The temperature rapidly rose to 20° and was controlled at this temperature during the addition. When the addition was complete the solution was stirred for 5 minutes and then added slowly to a mixture of ice and water (350 g). The precipitated solid was filtered off, washed thoroughly with water and dried in vacuo. The product was recrystallised from benzene with filtering to afford 2-phthalimido-N-(1,1,5-trimethylhexyl)acetamide, m.p. 162°-163°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04277498 |
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| Source dataset | uspto-grants-1981_07 |
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| ORD ID | ord-a48c9c223f89431c8439d70714812a71 |
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| Source note | uspto-grants-1981_07 |
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