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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6626Generated: October 25, 2026

Benzyl Chloride → 1-Phenyl-2,5,8,11-tetraoxatridecan-13-ol

https://huagongshe.com/reaction/6626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantTetraethylene GlycolHCID 8200—
ReactantSodium HydroxideHCID 14798—
SolventSodium ChlorideHCID 5234—
Product1-Phenyl-2,5,8,11-tetraoxatridecan-13-olHCID 1107695771%

Reaction Conditions

Temperature100 °C

Reaction Steps

To the oil of non-polydispersed tetraethylene glycol (19.4 g, 0.10 mol) was added a solution of NaOH (4.0 g in 4.0 mL) and the reaction was stirred for 15 mm. Then benzyl chloride (3.54 mL, 30.8 mmol) was added and the reaction mixture was heated to 100° C. and stirred overnight. The reaction mixture was cooled to room temperature, diluted with sat. NaCl (250 mL), and washed CH2Cl2 (2×200 mL). The organic layers were combined, washed sat. NaCl, dried MgSO4, and chromatographed (silica, ethyl acetate) to afford the non-polydispersed title compound as a yellow oil (6.21 g, 71% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084114B2
Source datasetuspto-grants-2006_08
ORD IDord-a1d63875a1484e9a87099c7b743dc497
Source noteuspto-grants-2006_08