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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280863Generated: October 31, 2026

1-Isopropylhydrazine hydrochloride → HCID 89370568, compound

https://huagongshe.com/reaction/2280863

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Isopropylhydrazine hydrochlorideHCID 85573—
ReactantHCID 89370582HCID 89370582—
SolventEthanolHCID 702—
ProductHCID 89370568HCID 89370568—

Reaction Steps

Compound 8b (6.29 g, 29.9 mmol) was dissolved in dry EtOH (65 mL, denaturated with 5% of MeOH) and isopropyl hydrazine hydrochloride (3.97 g, 35.9 mmol) was added. The reaction mixture was stirred for 3 h at rt. The solvent was removed and to the oily residue were added EA (100 mL), water (50 mL) and sat. NaHCO3 (50 mL) sequentially. The layers were separated and the aq. phase was re-extracted with EA (50 mL). The combined organic phases were washed with brine (70 mL) and dried over anh. Na2SO4. The solvent was removed under vacuum and the residue was dried under reduced pressure. Yield: 7.23 g (contains 3.4% of EtOAc by NMR, recalculated pure yield: 6.98 g, 94%). Crude product 8c is 98% pure by HPLC and NMR. 1H-NMR (CDCl3), δ (ppm): 6.62 (s, 1H), 4.88-4.82 (m, 2H), 4.42-4.32 (m, 3H), 3.56-3.45 (m, 1H), 3.17-3.07 (m, 2H), 2.88-2.79 (m, 2H), 1.49 (d, J=8.0 Hz, 6H), 1.37 (t, J=8.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139539B2
Source datasetuspto-grants-2015_09
ORD IDord-f9e3464fa29c45a2bd6622cda0141c6e
Source noteuspto-grants-2015_09