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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262828Generated: November 1, 2026

tert-Butyl bromoacetate → HCID 57426189, compound

https://huagongshe.com/reaction/2262828

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactantethyl 2,3-dihydro-1H-indene-2-carboxylateHCID 15280733—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 57426189HCID 57426189—

Reaction Steps

To a solution of ethyl indane-2-carboxylate (Schaaf et al., J. Med. Chem. 1983, 26, 328-334) (2.00 g, 10.5 mmol) in THF at −78° C. was added sodium bis(trimethylsilyl)amide (15.8 mL of a 1.0 M solution in THF, 15.8 mmol) dropwise, over 10 min. The mixture was stirred for 15 min, then tert-butyl bromoacetate (3.08 g, 15.8 mmol) was added dropwise, over 30 min. The resulting mixture was stirred for 30 min at −78° C., then poured into brine (20 mL) and extracted with EtOAc (50 mL). The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 90:10, to give the title compound. MS: m/z=368 (M+Na+CH3CN).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851464B2
Source datasetuspto-grants-2010_12
ORD IDord-ee789bf6d1fe4db9acf9e45f36223689
Source noteuspto-grants-2010_12