HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylphosphine → methyl 3-(2-chloro-6-fluorophenyl)-2-hydrazinylidene-3-oxopropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | Methyl 3-(2-chloro-6-fluorophenyl)-2-diazo-3-oxopropionate | HCID 86613890 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | methyl 3-(2-chloro-6-fluorophenyl)-2-hydrazinylidene-3-oxopropanoate | HCID 178501731 | 63.6% |
Reaction Steps
To 4.90 g (19.1 m=ol) of methyl 3-(2-chloro-6-fluorophenyl)-2-diazo-3-oxopropionate in 100 mL of diisopropyl ether was added 5.2 mL (21 mmol) of tributylphosphine. The bright yellow phosphazine adduct that precipitated from solution after 30 min. was collected, dissolved in dichloromethane and concentrated onto silica gel. The hydrazone product was eluted with a 75% hexanes/ethyl acetate mixture to give 3.14 g of the title compound as an off-white solid. The filtrate from the adduct formation was similarly loaded onto silica gel and eluted to give an additional 1.04 g of the title compound. An overall isolated yield of 4.18 g (85%) of the title compound as a 10:1 mixture of hydrazone isomers was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897607B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-d8e584d5c373422b99ed1d351089a974 |
| Source note | uspto-grants-2011_03 |