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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047695Generated: November 2, 2026

Oxalyl chloride → HCID 59314300, compound

https://huagongshe.com/reaction/1047695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,3-Dihydro-1-benzofuran-7-carboxylic acidHCID 2795014—
ReactantEthyl 2-amino-2,3-dihydro-1H-indene-2-carboxylateHCID 10921653—
SolventDichloromethaneHCID 6344—
ProductHCID 59314300HCID 5931430075.3%

Reaction Steps

To a solution of 2,3-dihydro-benzofuran-7-carboxylic acid (394 mg, 2.4 mmol) in DCM (10 mL) is added oxalyl chloride (0.85 mL, 9.6 mmol). The resulting solution is stirred at RT for 2 h. After the removal of DCM and excess oxalyl chloride, the residue, 2-amino-indan-2-carboxylic acid ethyl ester (500 mg, 2.4 mmol) and DIPEA (3.17 mL, 19.2 mmol) are dissolved in DCM (20 mL). The resulting solution is stirred at RT overnight. The reaction solution is diluted with DCM (40 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 (120 g silica gel, gradient elution: 0%-20% EtOAc in heptane) to give a pure product (39) as white solid (635 mg, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-f203d3d77bf448ffa6defc7818587ab4
Source noteuspto-grants-2013_10