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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047672Generated: October 31, 2026

Allyl bromide → 2-(3-Chloro-2-isopropoxy-benzoylamino)-indan-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1047672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantCesium carbonateHCID 10796—
Reactant2-(3-Chloro-2-hydroxy-benzoylamino)-indan-2-carboxylic acid ethyl esterHCID 59314122—
SolventDimethylformamideHCID 6228—
Product2-(3-Chloro-2-isopropoxy-benzoylamino)-indan-2-carboxylic acid ethyl esterHCID 5931434381.2%

Reaction Steps

To a suspension of 2-(3-chloro-2-hydroxy-benzoylamino)-indan-2-carboxylic acid ethyl ester (14) (150 mg, 0.42 mmol), anhydrous Cs2CO3 (274 mg, 0.84 mmol), and KI (13 mg, 0.08 mmol) in DMF (7 mL) is added 3-bromo-propene (237 μL, 2.52 mmol). The resulting reaction suspension is stirred at RT overnight. After the removal of DMF in vacuo, the residue is dissolved in EtOAc (20 mL) and washed with water (1×5 mL) and brine (2×5 mL). The organic layer is dried over anhydrous Na2SO4 and concentrated in vacuo. The residue is purified by flash column chromatography (80 g silica gel, gradient elution: 10-40% EtOAc in heptane) to give a pure product (15) as white solid (137 mg, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-b896bc6efc6b4b238cea9c8caf5c3dbd
Source noteuspto-grants-2013_10