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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635062Generated: November 3, 2026

tert-Butyl bromoacetate → HCID 53823464, compound

https://huagongshe.com/reaction/1635062

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 18675474HCID 18675474—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
ProductHCID 53823464HCID 53823464—

Reaction Steps

To a solution of (±)-(E)-N-(2-hydroxy-pent-3-enyl)-4-methoxybenzenesulfonamide (1.2 grams, 4.42 mmol) in tetrahydrofuran-dimethylformamide (10 mL, ca. 3:1) at 0° C. is added sodium bis(trimethylsilyl)amide (4.9 mL, 1.0 M solution in torahydrofuran). After 10 minutes, t-butylbromoacetate (786 mL, 4.83 mmol) is added. The mixture is warmed to room temperature, stirred for 1 hour and quenched with saturated ammonium chloride solution. The mixture is extracted with ethyl acetate and the combined extracts are dried (sodium sulfate), filtered and concentrated. The crude product is purified by silica gel chromatography (elution with 1:1 ethyl acetate-hexanes) to provide [(2-hydroxy-pent-3-enyl)-(4-methoxybenzenesulfonyl)-amino]-acetic acid t-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509337B1
Source datasetuspto-grants-2003_01
ORD IDord-1ee0577740f848f49127eebd6c460db1
Source noteuspto-grants-2003_01