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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067338Generated: October 31, 2026

Tin tetrachloride → [2-(4-Bromo-benzyl)-4,5-dimethyl-furan-3-yl]-(3,5-diisopropyl-4-methoxy-phenyl)-methanone

https://huagongshe.com/reaction/1067338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTin tetrachlorideHCID 24287—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 15895030HCID 15895030—
Reactant2-(4-Bromo-benzyl)-4,5-dimethyl-furanHCID 23445620—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product[2-(4-Bromo-benzyl)-4,5-dimethyl-furan-3-yl]-(3,5-diisopropyl-4-methoxy-phenyl)-methanoneHCID 2344561877.5%

Reaction Steps

The title compound was prepared according to the procedure in Example 5, step 2 using 3,5-diisopropyl-p-anisic acid (1.03 g, 4.35 mmol, RN-117439-59-5), oxalyl chloride (0.417 mL, 4.79 mmol), N,N-dimethylformamide (2 drops), tin (IV) chloride (0.560 mL, 4.79 mmol) and 2-(4-bromo-benzyl)-4,5-dimethyl-furan (1.15 g, 4.35 mmol) in CH2Cl2. Purification on Biotage KP-Sil eluting with 3% EtOAc/pet. ether gave 1.63 g (77%) of the title compound as a yellow clear oil. 1H NMR (DMSO-d6) δ1.16 (d, 12H), 1.80 (s, 3H), 2.19 (s, 3H), 3.28 (septet, 2H), 3.74 (s, 3H), 3.83 (s, 2H), 6.98 (d, 2H), 7.41 (dd, 2H), 7.44 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248764B1
Source datasetuspto-grants-2001_06
ORD IDord-39f08ba912f940caafd2914f1111de8d
Source noteuspto-grants-2001_06