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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017770Generated: October 31, 2026

tert-Butyl bromoacetate → HCID 22897435, compound

https://huagongshe.com/reaction/1017770

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 22885692HCID 22885692—
SolventAcetonitrileHCID 6342—
ProductHCID 22897435HCID 22897435—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 251 mg of 1-(S)-(1-(R)-(3,5-bis(trifluoromethyl)-phenyl)ethoxy)-2-(S)-(4-fluorophenyl)-3-(R)-(methylamino)cyclopentane from Example 15 in 6 mL of acetonitrile was added 0.108 mL of t-butyl bromoacetate and 0.36 mL of DIPEA. The reaction was heated at 50° C. for 5 hours and then concentrated in vacuo. The residue was diluted with water and extracted twice with ethyl acetate. The organic layers were washed with brine, dried with sodium sulfate, combined and evaporated. The residue was purified by FC (0-2.5% methanol in methylene chloride) to afford 294 mg of title compound. Mass spec (ESI): 564 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479518B2
Source datasetuspto-grants-2002_11
ORD IDord-7e2cf46bf19a47a889fb61e9cfa42d21
Source noteuspto-grants-2002_11