HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227272Generated: October 31, 2026
3-Bromo-2-methyl-1-propene → HCID 22086395, compound
https://huagongshe.com/reaction/2227272
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromo-2-methyl-1-propene | HCID 357785 | — |
| Reactant | HCID 22086394 | HCID 22086394 | — |
| Reactant | Lithim bis(trimethylsilylamide) | HCID 86588160 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22086395 | HCID 22086395 | — |
Reaction Steps
To a stirred solution of 2-2 (18 g, 54 mmol) in tetrahydrofuran (400 mL) at −78° C. under argon was added a solution of lithium bis(trimethylsilylamide) (70.2 mL of a 1.0 M solution in tetrahydrofuran) over 20 min. After an additional 20 min., 3-bromo-2-methylpropene (14.6 g, 108 mmol) was added in one portion. After 20 min., the reaction mixture was allowed to warm to 0° C. After 3.5 h, the reaction mixture was diluted with ethyl acetate, washed with water, saturated aqueous sodium hydrogen carbonate, saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate. The reaction mixture was filtered and concentrated at reduced pressure. The resulting oil (3-1) was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06413955B1 |
|---|
| Source dataset | uspto-grants-2002_07 |
|---|
| ORD ID | ord-43d4f223c6f94608834a7f2a5edff178 |
|---|
| Source note | uspto-grants-2002_07 |
|---|