HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 13885860, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 13885857 | HCID 13885857 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13885860 | HCID 13885860 | — |
Reaction Steps
A slurry of sodium hydride (168 mg, 4.2 mmole, 60% in mineral oil dispersion) in 5 ml of dry tetrahydrofuran at 0° C. under argon was treated dropwise with 1,4-dihydro-2-[[(4-methoxyphenyl)methyl]thio]-6-methyl-4-(3-nitrophenyl)-5-pyrimidinecarboxylic acid, methyl ester in 15 ml of dry tetrahydrofuran. After an additional 10 minutes at 0° C., allyl bromide was added and the reaction mixture was allowed to warm to room temperature overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04684655 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-d76b34220cb74d5c9ef8c5b1ac5cef9c |
| Source note | uspto-grants-1987_08 |