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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984128Generated: October 31, 2026

Methyl bromoacetate → HCID 20765987, compound

https://huagongshe.com/reaction/984128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl bromoacetateHCID 60984—
Reactant6-Methoxy-1,2-benzisoxazol-3(2H)-oneHCID 11412577—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20765987HCID 2076598743.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867224B2
Source datasetuspto-grants-2005_03
ORD IDord-f3afd7220bd44eada58242f247fe0ed3
Source noteuspto-grants-2005_03