HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57405Generated: October 29, 2026
4-Chlorobenzoyl chloride → HCID 90454299, compound
https://huagongshe.com/reaction/57405
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | tert-butyl N-((1S)-1-(hydrazinecarbonyl)ethyl)carbamate | HCID 10241974 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 90454299 | HCID 90454299 | 92.2% |
Reaction Steps
4-Chlorobenzoyl chloride (0.63 mL, 4.92 mmol, 1.0 equiv) was added to a solution of (S)-tert-butyl(1-hydrazinyl-1-oxopropan-2-yl)carbamate (1.0 g, 4.92 mmol) in DCM (25 mL) at 0° C. A white precipitate formed. The mixture was stirred at 0° C. for 1 hour and the reaction mixture was then concentrated in vacuo to give crude (S)-tert-butyl(1-(2-(4-chlorobenzoyl)hydrazinyl)-1-oxopropan-2-yl)carbamate (1.55 g), which was used without purification. 1H NMR (400 MHz, CD3OD) δ 7.85 (d, J=8.7 Hz, 2H), 7.49 (d, J=8.7 Hz, 2H), 4.21 (q, J=7.0 Hz, 1H), 1.45 (s, 9H), 1.41 (d, J=7.2 Hz, 3H). MS m/z 342.1 (M+H)+; Rt-0.69 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434719B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-8f86b7e42ff34544ae56671e63771a17 |
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| Source note | uspto-grants-2016_09 |
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