Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1,4-dihydro-3H-2-benzopyran-3-one | HCID 78092 | — |
| Reactant | N'-methyl(tert-butoxy)carbohydrazide | HCID 15671306 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86758393 | HCID 86758393 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06432944B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-51fed0c6f1b849978a8940cef17adbd9 |
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| Source note | uspto-grants-2002_08 |
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