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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170834Generated: November 1, 2026

Phthalic Anhydride → HCID 59767867, compound

https://huagongshe.com/reaction/1170834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 66846189HCID 66846189—
SolventTolueneHCID 1140—
ProductHCID 59767867HCID 59767867100%

Reaction Steps

A solution of (S)-hexahydro-pyridazine-3-carboxylic acid methyl ester hydrochloride (Y. Nakamura, C. J Shin, Chem. Lett, 1991, 11, 1953-1956) (370 mg, 2.05 mmol), phthalic anhydride (318 mg, 2.15 mmol) and diisopropylethylamine (291 mg, 2.25 mmol) was heated in toluene (5 mL) for 2 h. The reaction mixture was then cooled and partitioned between ethyl acetate and dilute HCl. The organic phase was washed with saturated aq. NaHCO3, dried (MgSO4), filtered and evaporated. The residue was crystallised from hexane and filtered to afford the title compound as a white solid (562 mg, 82%): 1H NMR (400 MHz, CD3OD) δ 1.59 (1H, m), 1.96 (1H, m), 2.17 (1H, m), 2.55 (1H, m), 3.38 (1H, m), 3.70 (3H, s), 4.89 (1H, m), 5.74 (1H, m), 7.89 (2H, m), 8.16 (2H, m). 13C NMR (100 MHz, CD3OD) δ 21.2 (CH2), 25.7 (CH2), 46.0 (CH2), 53.8 (CH), 58.1 (CH3), 129.0 (CH), 129.1 (CH), 130.1 (C), 130.6 (C), 135.3 (CH), 135.7 (CH), 160.4 (C), 162.4 (C), 171.7 (C).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829561B2
Source datasetuspto-grants-2010_11
ORD IDord-bbbeb34e4bed46679e0c039fd64567ad
Source noteuspto-grants-2010_11