HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 886071Generated: October 30, 2026
Ethyl 2-chloroacetoacetate → Chloro-(5-bromo-2-but-3-ynyloxyphenylhydrazono)acetic acid ethyl ester
https://huagongshe.com/reaction/886071
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 2-chloroacetoacetate | HCID 11858 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 5-Bromo-2-but-3-ynyloxy-phenylamine | HCID 58204909 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | Chloro-(5-bromo-2-but-3-ynyloxyphenylhydrazono)acetic acid ethyl ester | HCID 86652298 | 95% |
Reaction Steps
2-Chloro-3-oxo-butyric acid ethyl ester (1.94 g, 11.2 mmol) and sodium acetate (1.45 g, 17.8 mmol) were stirred in IMS (100 mL) to give a clear solution, then cooled to 0° C. Separately, 5-bromo-2-but-3-ynyloxy-phenylamine (2.68 g, 11.2 mmol) in 6M hydrochloric acid (6.8 mL) was cooled to 0° C. and a solution of sodium nitrite (0.77 g, 11.2 mmol) in water (11.2 mL) was added dropwise with stirring, keeping the temperature below 5° C. The aqueous acidic solution was added to the IMS solution, washed in with a little water, keeping the temperature below 5° C. After 1 h at 0-5° C., the mixture was diluted with water and extracted several times with ethyl acetate. The combined organic extracts were washed with water, dried (Na2SO4), filtered and concentrated in vacuo to give Chloro-(5-bromo-2-but-3-ynyloxyphenylhydrazono)acetic acid ethyl ester as a pale brown solid (3.96 g, 95%). LCMS: RT=4.97 min, [M+Na]+=395/397/399.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242104B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-56f06394b92149a0b13ab971361c266f |
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| Source note | uspto-grants-2012_08 |
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