HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971732Generated: November 1, 2026
Hydrochloric Acid → 2-(Tert-butyl(hex-5-ynyl)amino)-2-oxoacetic acid
https://huagongshe.com/reaction/1971732
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 2-(tert-butyl(hex-5-ynyl)amino)-2-oxoacetate | HCID 58124820 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(Tert-butyl(hex-5-ynyl)amino)-2-oxoacetic acid | HCID 58124934 | 80.3% |
Reaction Steps
A solution of 0.7 g of 17d in 8 ml of dioxane was mixed with a solution of 0.3 g of KOH in 3 ml of water. The mixture was stirred for 2 h at 50° C. and then diluted with 30 ml of water and acidified to pH3 with 0.5 N HCl. The product was extracted with ethyl acetate. The extract was washed with water, dried and concentrated, to give 0.50 g of 19a as a colorless oil. NMR (CDCl3) δ 1.53 (s and m, 11, tertC4H9 and CH2), 1.78 (m, 2, CH2), 1.97 (t, 1, acetylene), 2.20 (m, 2, CH2), 3.56 (m, 2, CH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431564B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-3d10eeb7b7ad4f7bb4577dd8e992ae6f |
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| Source note | uspto-grants-2013_04 |
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