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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871295Generated: November 1, 2026

Acetone cardice → (2-Ethyl-benzofuran-3-yl)-(2'-hydroxy-[1,1';3',1"]terphenyl-5'-yl)-methanone

https://huagongshe.com/reaction/1871295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetone cardiceHCID 18522661—
ReactantBoron tribromide dichloromethaneHCID 22277759—
Reactant(2-Ethyl-benzofuran-3-yl)-(2'-methoxy-[1,1';3',1"]terphenyl-5'-yl)-methanoneHCID 23445613—
SolventDichloromethaneHCID 6344—
Product(2-Ethyl-benzofuran-3-yl)-(2'-hydroxy-[1,1';3',1"]terphenyl-5'-yl)-methanoneHCID 2344563483%

Reaction Steps

At -78° C., to a stirred solution of (2-ethyl-benzofuran-3-yl)-(2'-methoxy-[1,1';3',1"]terphenyl-5'-yl)-methanone (1.07 g, 2.47 mmol) in CH2Cl2 (10.1 mL) was added dropwise 1M boron tribromide/CH2Cl2 (5.2 mL). After the addition was complete, the dry ice/acetone bath was replaced with an ice water bath and the reaction was stirred for 72 h, eventually warming to ambient temperature. The reaction was carefully quenched with crushed ice, diluted with H2O (16 mL) and extracted with ether. The ethereal extracts were dried (MgSO4) and concentrated. Purification on Biotage KP-Sil eluting with 15% acetone/hexane gave 0.86 g, (83%) of the title compound as a white solid, mp 142-143° C. 1H NMR (DMSO-d6) δ 1.24 (t, 3 H), 2.90 (quartet, 2 H), 7.28-7.66 (m, 16 H), 9.37 (s, 1 H). IR (KBr) 3200, 2950, 1625, 1560 and 1175 cm-1. mass spectrum (EI), m/z 418 (M+). Anal. Calcd. for C29H22O3.0.35H2O: C, 82.00; H, 5.39; N, 0.00. Found: C, 82.06; H, 5.40; N, 0.07.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06103708
Source datasetuspto-grants-2000_08
ORD IDord-e05d4c3529fc4a0abd8be7d0e9993e58
Source noteuspto-grants-2000_08