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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280883Generated: October 30, 2026

Tin tetrachloride → (2-Ethyl-benzofuran-3-yl)-(2'-methoxy-[1,1';3',1"]terphenyl-5'-yl)-methanone

https://huagongshe.com/reaction/1280883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTin tetrachlorideHCID 24287—
ReactantOxalyl chlorideHCID 65578—
Reactant2-EthylbenzofuranHCID 76582—
Reactant2'-Methoxy-[1,1';3',1"]terphenyl-5'-carboxylic acidHCID 23445632—
SolventDichloromethaneHCID 6344—
Product(2-Ethyl-benzofuran-3-yl)-(2'-methoxy-[1,1';3',1"]terphenyl-5'-yl)-methanoneHCID 2344561373%

Reaction Steps

The title compound was prepared according to the procedure in Example 5, step 2 using 2′-methoxy-[1,1′;3′,1″]terphenyl-5′-carboxylic acid (1.031 g, 3.388 mmol), oxalyl chloride (0.325 mL, 3.727 mmol), commercial 2-ethylbenzofuran (0.4953 g, 3.388 mmol) and tin (IV) chloride (0.436 mL, 3.727 mmol) in CH2Cl2. Purification on Biotage KP-Sil eluting with 3% EtOAc/pet. ether gave 1.070 g, (73%) of the title compound. 1H NMR (DMSO-d6) δ 1.24 (t, 3H), 2.90 (quartet, 2H), 3.21 (s, 3H), 7.30-7.67 (m, 14H), 7.75 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451845B1
Source datasetuspto-grants-2002_09
ORD IDord-ca1c38c5d36f46f4965af473385c73d5
Source noteuspto-grants-2002_09