HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetyl bromide → N-[4-(aminosulfonyl)-2-chlorophenyl]-2-bromoAcetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Amino-3-chlorobenzenesulfonamide | HCID 1502014 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[4-(aminosulfonyl)-2-chlorophenyl]-2-bromoAcetamide | HCID 59511722 | — |
Reaction Steps
A mixture of 750 mg (3.63 mmol) of 4-amino-3-chlorobenzenesulfonamide (A-2) and 610 mg (7.26 mmol) of sodium bicarbonate in 25 mL of CH2Cl2 was stirred at room temperature for 18 hours. Bromoacetyl bromide (A-1) was then added, and the mixture was stirred for an additional 12 hours. The mixture was then concentrated in vacuo to a yellow oil. The oil was washed with three 25 mL portions of diethyl ether, decanted, and concentrated in vacuo to give the desired product A-3 as a tan solid. MS: M+1=329.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07807684B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-b0b60f6f4238438b970beae9d54a4270 |
| Source note | uspto-grants-2010_10 |