HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324795Generated: October 26, 2026
Isopropanol → Ethyl 3-amino-4-methyl-pent-2-enoate
https://huagongshe.com/reaction/324795
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Product | Ethyl 3-amino-4-methyl-pent-2-enoate | HCID 59557418 | — |
Reaction Steps
To 100 g (0.63 mol) of ethyl isobutyryl acetate was added ammonium acetate (68.2 g, 0.89 mol), cyclohexane (230 mL) and isopropanol (74 mL). The mixture was heated at reflux under argon atmosphere with a Dean-Stark trap. After 2 hours, a second portion of ammonium acetate (14.6 g, 0.19 mol) was added to the reaction. The reaction was heated at reflux for 12 hours and then allowed to cool to room temperature. A total of ˜30 mL of water was collected in the Dean-Stark trap. An ice bath was used to cool the reaction to 10° C. and then ammonium hydroxide (63 mL) was added dropwise. The organic layer was separated, dried with sodium sulfate, filtered, and concentrated to yield a yellow oil. The crude product (90.9 g, 0.58 mol, 92%) was taken directly to the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06218431B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-6d860f2537824a04963bbe31dafe5a49 |
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| Source note | uspto-grants-2001_04 |
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