HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179482Generated: October 30, 2026
N,N-Dimethylaniline → (2e)-3-{2,6-Difluoro-4-[(isopropoxycarbonyl)amino]phenyl}prop-2-enyl diazoacetate
https://huagongshe.com/reaction/1179482
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Glyoxylyl Chloride p-toluenesulfonylhydrazone | HCID 57296158 | — |
| Reactant | isopropyl 3,5-difluoro-4-[(1E)-3-hydroxyprop-1-enyl]phenylcarbamate | HCID 58978084 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2e)-3-{2,6-Difluoro-4-[(isopropoxycarbonyl)amino]phenyl}prop-2-enyl diazoacetate | HCID 131726632 | — |
Reaction Steps
Glyoxylic acid chloride p-toluenesulfonylhydrazone (4.64 g, 17.8 mmol) was added to a suspension of isopropyl 3,5-difluoro-4-[(1E)-3-hydroxyprop-1-enyl]phenylcarbamate (2.68 g, 9.89 mmol) in dichloromethane (66 mL). The mixture was cooled to 0° C. and treated with N,N-dimethylaniline (2.26 mL, 17.8 mmol). After 30 minutes, triethylamine (6.89 mL, 49.5 mmol) was added and the mixture stirred 30 minutes at 0° C. and 15 minutes at room temperature. The reaction mixture was then concentrated to ca. 15 mL and 50 mL of water added. The mixture was extracted with two portions of diethyl ether and the combined organic solutions washed with saturated NaHCO3, brine, and dried (MgSO4), filtered and concentrated. Purification by column chromatography (0-25% ethyl acetate-hexane) provided the title compound a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07279494B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-17a464035f7b48108458ace76583064d |
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| Source note | uspto-grants-2007_10 |
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