HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → Methyl 3-bromomethyl-2-chloro-4-methylsulfonylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 2-chloro-3-methyl-4-methylsulfonylbenzoate | HCID 15132838 | — |
| Product | Methyl 3-bromomethyl-2-chloro-4-methylsulfonylbenzoate | HCID 10969914 | — |
Reaction Steps
80 g (0.3 mol) of methyl 2-chloro-3-methyl-4-methylsulfonylbenzoate, 54 g (0.31 mol) of N-bromosuccinimide and 1.5 g of azoisobutyronitrile are stirred at 76° C. for 6 h. The reaction mixture is filtered and freed form the solvent under reduced pressure. Yield: 104 g; m.p. 83-85° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06432881B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-52162fff8047469d9d63b1f0814f3506 |
| Source note | uspto-grants-2002_08 |