HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991995Generated: October 26, 2026
Diisopropylamine → N,N-Diphenyl-N'-(2-chlorophenyl)hydrazine
https://huagongshe.com/reaction/991995
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Hydrazine, 1,1-diphenyl-, hydrochloride (1:1) | HCID 10738 | — |
| Reactant | 1-Bromo-2-chlorobenzene | HCID 12754 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Binap, (A+-)- | HCID 634876 | — |
| Catalyst | Palladium (II) acetate | HCID 4144353 | — |
| Product | N,N-Diphenyl-N'-(2-chlorophenyl)hydrazine | HCID 18415148 | 74% |
Reaction Steps
1,1-Diphenylhydrazine hydrochloride (1.2 equiv., 0.6 mmol, 135 mg), 2-chlorobromobenzene (1.0 equiv., 0.5 mmol, 0.06 mL), Pd(OAC)2 (0.05 equiv, 0.025 mmol, 6 mg), BINAP (0.05 equiv., 0.025 mmol, 16 mg), and NaOtBu (1.4 equiv., 0.7 mmol, 67 mg) and diisopropylamine (2 mL) were added to an oven dried test tube which was capped with a septum and purged briefly with argon (˜1 min.) and then heated to 80° C. for 5 hours. The reaction was then cooled to room temperature, diluted with Et2O (2 mL), filtered through Celite and concentrated under vacuum. The crude mixture was purified by flash column chromatography (2% EtOAc/Hex) to give the title product as a white solid (109 mg, 0.37 mmol, 74% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06465693B2 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-1ad8f40cc69349b58e774d48ed8588c1 |
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| Source note | uspto-grants-2002_10 |
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