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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880577Generated: November 2, 2026

Phenylhydrazine hydrochloride → HCID 11852744, compound

https://huagongshe.com/reaction/1880577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazine hydrochlorideHCID 60962—
ReactantHCID 86761703HCID 86761703—
CatalystZincchlorideHCID 3007855—
SolventAcetic AcidHCID 176—
ProductHCID 11852744HCID 11852744—

Reaction Conditions

Temperature80 °C

Reaction Steps

A glacial acetic acid solution (4 mL) containing the intermediate from Step C (150 mg, 0.27 mmol), phenyl hydrazine hydrochloride (51 mg, 0.35 mmol) and ZnCl2 (110 mg, 0.81 mmol) was heated at 80° C. for 1 hour. The solution was concentrated and partitioned between aqueous 1N HCl and ethyl acetate. The organic phase was washed with brine, dried over MgSO4, filtered and concentrated. The residue was purified by RP-HPLC and the isolated material was resolved using chiral OJ SFC-HPLC to give the title compounds. Isomer A: Chiral LC1 4.85 min, LCMS1 3.80 min. (M+H)=572. Isomer B: Chiral LC1 12.09 min, LCMS1 3.80 min. (M+H)=572. Representative 1H NMR (400 MHz, CD3OD): δ 7.58 (d, J=8.2 Hz, 2H); 7.47 (d, J=8.6 Hz, 2H); 7.37-7.14 (m, 11H); 7.01 (t, J=7.5 Hz, 1H); 6.85 (t, J=7.5 Hz, 1H); 4.57 (t, J=7.9 Hz, 1H); 3.63 (dd, J=6.7, 13.4 Hz, 1H); 3.56 (t, J=6.9 Hz, 2H); 3.36 (dd, J=9.1, 13.3 Hz, 1H); 2.57 (t, J=7.0 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318760B2
Source datasetuspto-grants-2012_11
ORD IDord-8e436370929a4f32baac6ec260f45815
Source noteuspto-grants-2012_11