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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096829Generated: October 26, 2026

Tributylphosphine → 2-[2-(2,6-Dichloro-4-methylphenoxy)ethoxy]thiazole

https://huagongshe.com/reaction/1096829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant2,6-Dichloro-4-methylphenolHCID 17077—
Reactant2-(Thiazol-2-yloxy)ethanolHCID 45121950—
SolventTolueneHCID 1140—
Product2-[2-(2,6-Dichloro-4-methylphenoxy)ethoxy]thiazoleHCID 6678358469%

Reaction Steps

A mixture of 2-(thiazol-2-yloxy)ethanol (6.39 g, 44.0 mmol), 2,6-dichloro-p-cresol (15.6 g, 88.0 mmol), azodicarboxylic-dipiperidide (22.2 g, 88.0 mmol) and PBu3 (85%, 38.3 mL, 132 mmol) in toluene (325 mL) was heated to reflux for 30 min. The mixture was allowed to cool to rt, filtered, and the precipitate was washed thoroughly with toluene. The filtrate was evaporated under reduced pressure. The residue was diluted with EtOAc, and washed with aq. 1M NaOH (4×). The org. phase was dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the crude by FC (EtOAc/heptane 1:19→1:9→1:4) yielded the title compound as a colourless solid (9.24 g, 69%). LC-MS: tR=1.06 min, ES+: 304.05.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138340B2
Source datasetuspto-grants-2012_03
ORD IDord-bb51e01ccef1426a8f2a62160c0117c6
Source noteuspto-grants-2012_03