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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888750Generated: October 26, 2026

1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) → 1-(Bis(4-methoxyphenyl)(phenyl)methoxy)icosan-3-ol

https://huagongshe.com/reaction/888750

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
ReactantIcosane-1,3-diolHCID 25229601—
SolventPyridineHCID 1049—
Product1-(Bis(4-methoxyphenyl)(phenyl)methoxy)icosan-3-olHCID 68748764—

Reaction Steps

Icosane-1,3-diol (3.7 g, 11.8 mmoles) is co-evaporated twice with anhydrous pyridine (50 mL each) and then is dissolved in anhydrous pyridine (60 mL). The solution is chilled in an ice bath, and 4,4′-dimethoxytritylchloride (4.2 g, 12.4 mmoles) is added. The reaction is allowed to warm to ambient temperature and is stirred for 16 hours. The remaining 4,4′-dimethoxytritylchloride is quenched with methanol (10 mL), and the yellow solution is then evaporated to near dryness. The residue is co-evaporated twice to dryness with toluene (50 mL each). The crude product is purified on silica gel (150 mL bed volume) eluting with hexanes:acetone:triethylamine (95.5:5:0:5 [v/v/v], 500 mL). Fractions containing pure product by thin layer chromatography are pooled and evaporated to a pale yellow syrup. The syrup is dried well in vacuo. The yield is 6.8 g (93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252755B2
Source datasetuspto-grants-2012_08
ORD IDord-61b24554aebc4cbe929c36645479185c
Source noteuspto-grants-2012_08