HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl bromoacetate → HCID 20765987, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | 6-Methoxy-1,2-benzisoxazol-3(2H)-one | HCID 11412577 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20765987 | HCID 20765987 | 43.5% |
Reaction Steps
The KN(TMS)2 (7.2 g) was added to a solution of compound 22B (4 g) in 150 mL of THF at 0° C. by portion, another one hour at 0° C. with stirring. Methyl bromoacetate (7 g) was added, stirred at RT overnight. The reaction mixture was quenched with 150 mL of ethyl acetate and 100 mL of 2N HCl. The organic layer was separated, washed with water, brine, dried (MgSO4), concentrated to afford an off-white solid compound 22C (2.5 g). mp 185-188° C.; MS: 238 (M+1)+. Preparation of 5-Chlorosulfonyl-6-methoxy-3-oxo-3H-benzo[d]isoxazol-2-yl-acetic acid methyl ester (Compound 22D)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06867224B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-f3afd7220bd44eada58242f247fe0ed3 |
| Source note | uspto-grants-2005_03 |