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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120022Generated: November 1, 2026

HCID 14937397, compound → HCID 15399808, compound

https://huagongshe.com/reaction/2120022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14937397HCID 14937397—
ReactantHCID 23437329HCID 23437329—
CatalystFerrous ChlorideHCID 24458—
SolventDichloromethaneHCID 6344—
ProductHCID 15399808HCID 1539980867%

Reaction Steps

Anhydrous iron chloride (4.7 g, 28.9 mmol) was added to a stirred mixture of 2-acetoxy-1-hexyloxybenzene (3.4 g, 14.4 mmol) and 3,3′,4,4′-tetrahexyloxybiphenyl (4.0 g, 7.2 mmol) in dichloromethane. The mixture was stirred for 5 h and poured onto methanol (300 ml). The resultant precipitate was filtered off and saponified with potassium carbonate in ethanol (5% water) under reflux for over night. After cooling, water (50 ml) was added and the product was extracted with dichloromethane, dried (MgSO4), concentrated and purified by column chromatography on silica gel using dichloromethane and petroleum spirit (1:1) as eluent and then recrystallised from ethanol to yield a white solid (3.59 g, 67%). Found: C, 77.30; H, 9.85. C48H72O6 requires C, 77.38; H, 9.74. δH (CHCl3) 7.96 (s, 1H, ArH), 7.83-7.82 (m, 4H, ArH), 7.77 (s, 1H, ArH), 5.92 (1H, s, OH), 4.31-4.18 (m, 10H, OCH2), 1.99-1.92 (m, 10H, CH2), 1.58-1.55 (m, 10H, CH2), 1.46-1.38 (m, 20H, CH2), 0.97-0.83 (15H, m, CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689290B2
Source datasetuspto-grants-2004_02
ORD IDord-2bd98c1d2c6d4a1693d27025ae786f9c
Source noteuspto-grants-2004_02