HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585571Generated: October 27, 2026
Ammonium Chloride → Tert-butyl 5-amino-3,3-dimethyl-5-oxopentanoate
https://huagongshe.com/reaction/585571
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | 5-(Tert-butoxy)-3,3-dimethyl-5-oxopentanoic acid | HCID 15631255 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 5-amino-3,3-dimethyl-5-oxopentanoate | HCID 21927924 | 82% |
Reaction Steps
5-Tert-butoxy-3,3-dimethyl-5-oxopentanoic acid (6 g, 27.8 mmol) was dissolved in DMF (111 mL) and benzotriazol-1-yloxytris(pyrrolidino)phosphonium hexafluorophosphate (21.68 g, 41.7 mmol), 1-hydroxybenzotriazole (5.6 g, 41.7 mmol), diisopropylethylamine (19.3 mL, 111 mmol) and ammonium chloride (3 g, 55.6 mmol) were added. The mixture was stirred at room temperature for two hours. The DMF was removed under reduced pressure and the residue dissolved in ethyl acetate. The ethyl acetate was washed with 1N KHSO4, saturated sodium bicarbonate, brine, dried (Na2SO4) and concentrated. The residue was again dissolved in ethyl acetate, washed with 0.1N HCl, 0.1N NaOH, H2O, dried (Na2SO4), passed through a pad of silica and concentrated to give 4.9 g (82%) of the desired product. 1H NMR (DMSO-d6) 7.19 (br s, 1H), 6.71 (br s, 1H), 2.23 (s, 2H), 2.08 (s, 2H), 1.4 (s, 9H), 1.02 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06933304B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-e8bca9f807c24725bb001c9ca2d05c4a |
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| Source note | uspto-grants-2005_08 |
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