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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645281Generated: October 30, 2026

6-bromo-1'-pentylspiro[1-benzofuran-3,3'-indol]-2'(1'H)one → 1'-pentylspiro[1-benzofuran-3,3'-indol]-2'(1'H)-one

https://huagongshe.com/reaction/645281

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-bromo-1'-pentylspiro[1-benzofuran-3,3'-indol]-2'(1'H)oneHCID 59263436—
CatalystPalladiumHCID 23938—
SolventEthylacetate methanolHCID 21584119—
Product1'-pentylspiro[1-benzofuran-3,3'-indol]-2'(1'H)-oneHCID 5926341497%

Reaction Steps

A mixture of 6-bromo-1′-pentylspiro[1-benzofuran-3,3′-indol]-2′(1′H)-one (0.10 g, 0.27 mmol) and palladium/carbon (0.09 g, 0.01 mmol) in methanol/ethyl acetate (1/1, 4.00 mL) was stirred under hydrogen at atmospheric pressure for 16 h. The solvent was evaporated and the black residue was subjected to column chromatography (ethyl acetate/hexane, 1/6) to give the title compound (0.08 g, 97%) as a white solid: 1H NMR (300 MHz, CDCl3) δ 7.30 (dd, 1H), 7.18 (dd, 1H), 7.20 (d, 1H), 7.02 (dd, 1H), 6.96-6.90 (m, 2H), 6.79 (dd, 1H), 6.69 (d, 1H), 4.93 (d, 1H), 4.67 (d, 1H), 3.89-3.64 (m, 2H), 1.81-1.66 (m, 2H), 1.44-1.31 (m, 4H), 0.92 (t, 3H); 13C NMR (75 MHz, CDCl3) δ 177.2, 160.7, 142.5, 132.8, 129.7, 129.0, 128.8, 123.9, 123.3, 123.1, 121.3, 110.4, 108.6, 58.1, 40.4, 29.0, 27.2, 22.3, 14.0; MS (ES+) m/z 308.5 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700641B2
Source datasetuspto-grants-2010_04
ORD IDord-3c798a1ca2e14d4896312112d57a64a5
Source noteuspto-grants-2010_04