HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526379Generated: November 1, 2026
Diisopropylamine → HCID 71258941, compound
https://huagongshe.com/reaction/526379
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | tert-Butyl acetate | HCID 10908 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-Bromonicotinonitrile | HCID 736793 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 71258941 | HCID 71258941 | 34.3% |
Reaction Steps
Diisopropylamine (9.2 mL, 65 mmol) was added at 0° C. to a 3M solution of ethyl magnesium bromide in diethyl ether (10.9 mL, 32.7 mmol) and additional diethyl ether (20 mL). After one hour at 0° C. tert-butyl acetate (4.3 mL, 32.7 mmol) was added and stirring was continued for 30 minutes. 5-Bromopyridine-3-carbonitrile (2.0 g, 10.9 mmol) in diethyl ether (42 mL) was added at 0° C. After two hours at 0° C. saturated aqueous ammonium chloride solution was added. Phases were separated and the aqueous phase was extracted with diethyl ether. The combined extracts were washed with brine and dried over sodium sulfate. The solution was concentrated under reduced pressure and the residue was purified by chromatography on silica gel (ethyl acetate in hexane, 0 to 60%) to yield 1.12 g tert-butyl 3-amino-3-(5-bromopyridin-3-yl)prop-2-enoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09345793B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-85e5ba5a9d284d67b224e6a986e5a340 |
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| Source note | uspto-grants-2016_05 |
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