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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51369Generated: October 30, 2026

tert-Butyl bromoacetate → {9-[(3-Phenoxyphenyl)methyl]-5-carbamoylcarbazol-4-yl}oxyacetic acid, tert-butyl ester

https://huagongshe.com/reaction/51369

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant9-[(3-Phenoxyphenyl)methyl]-4-hydroxy-5-carbamoyl carbazoleHCID 22740765—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product{9-[(3-Phenoxyphenyl)methyl]-5-carbamoylcarbazol-4-yl}oxyacetic acid, tert-butyl esterHCID 8675626265.3%

Reaction Steps

40% Methanolic Triton B (0.054 mL, 0.12 mM) was added to a solution of the 9-[(3-phenoxyphenyl)methyl]-4-hydroxy-5-carbamoyl carbazole (39.5 mg, 0.10 mM) in 3 mL DMF at room temperature. After 3 minutes, t-butyl bromoacetate (54.8 mg, 0.27 mM) was added and the resultant mixture stirred at room temperature for 5 hours. The mixture was diluted with ethyl acetate, washed four times with H2O, once with saturated brine, dried over magnesium sulfate, filtered, and concentrated. The residue was purified by column chromatography on silica gel (elution with gradient methylene chloride/ethyl acetate) to afford 33.0 mg (65%) of the {9-[(3-phenoxyphenyl)methyl]-5-carbamoylcarbazol-4-yl}oxyacetic acid, tert-butyl ester as a white solid. 1H NMR (DMSO-d6) δ7.6 (d, 1H, J=8 Hz), 7.5-6.8 (m, 15H), 6.55 (d, 1H, J=8 Hz), 5.7 (s, 2H), 4.8 (s, 2H), and 1.45 (s, 9H). IR (KBr, cm−1) 3450, 1748, 1670, 1582, 1486, 1246, 1225, and 1151. MS (ES) m/e 523.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713645B1
Source datasetuspto-grants-2004_03
ORD IDord-63fb6ccb5b844c33a25d50992a8c7330
Source noteuspto-grants-2004_03