HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroformate → Methyl hept-6-en-2-ynoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | 3-Chloro-1-propyne | HCID 12221 | — |
| Reactant | HCID 178455850 | HCID 178455850 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl hept-6-en-2-ynoate | HCID 59644062 | 44% |
Reaction Steps
A solution of allylmagnesium bromide (1M, 150 mL, 150 mmol) in ether under a nitrogen atmosphere was cooled to −10° C., and propargyl chloride (5.4 mL, 75 mmol) was added dropwise. The solution was stirred for 24 h at room temperature, and then cooled to 0° C. Methyl chloroformate was added dropwise, and the solution was allowed to stir at room temperature for 4 h. The reaction was quenched by cautious addition of satd aq NH4Cl (100 mL) at 0° C. The organic layer was washed with brine, dried, and evaporated to a residue. Chromatography on silica gel provided the title compound (4.5 g, 44%) as a pale yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07666861B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-2beb62d89a934b15a71321753b2ccb5b |
| Source note | uspto-grants-2010_02 |