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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669671Generated: October 30, 2026

tert-Butyl bromoacetate → HCID 57426189, compound

https://huagongshe.com/reaction/1669671

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) drop wise over 10 min. The mixture was stirred for 15 min, then tert-butyl bromoacetate (3.08 g, 15.8 mmol) was added drop wise 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 numberUS07989624B2
Source datasetuspto-grants-2011_08
ORD IDord-71390979dbfe468aad5d587c1d519b18
Source noteuspto-grants-2011_08