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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2302276Generated: October 25, 2026

Acetic Acid → HCID 86758393, compound

https://huagongshe.com/reaction/2302276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1,4-dihydro-3H-2-benzopyran-3-oneHCID 78092—
ReactantN'-methyl(tert-butoxy)carbohydrazideHCID 15671306—
SolventEthyl AcetateHCID 8857—
ProductHCID 86758393HCID 86758393—

Reaction Conditions

Temperature100 °C

Reaction Steps

N-(t-Butoxycarbonyl)-N′-methylhydrazine (100 mmol) (Lenman, et al., J. Chem. Soc. Perkin Trans., 1997, 16, 2297-2312; Dutta, et al., J. Chem. Soc. Perkin Trans., 1986, 1655-1664) was added to 3-isochromanone (7.4 g, 50 mmol) (Cheng, et al., J. Heterocyclic Chem., 1995, 32, 73) in a sealed tube followed by 0.2 mL of acetic acid and heated for 12 h at 100° C. The reaction mixture was diluted with EtOAc (100 mL), washed with water (50 mL),1 M HCl (50 mL), brine (50 mL) and dried (Na2SO4). The desired alcohol 2-[2-[2-(Hydroxymethyl)phenyl]-1-oxoethyl]-2-methylhydrazinecarboxylic acid, 1,1-dimethylethyl ester was purified by flash chromatography (silica) using 50% EtOAc in hexane as eluent. MS (ESI) 295 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432944B1
Source datasetuspto-grants-2002_08
ORD IDord-51fed0c6f1b849978a8940cef17adbd9
Source noteuspto-grants-2002_08