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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528477Generated: October 26, 2026

2-tert-Butyloxirane → HCID 86711759, compound

https://huagongshe.com/reaction/528477

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-tert-ButyloxiraneHCID 92174—
Reactant2,4,6-Trichloropyrimidin-5-olHCID 86667332—
ProductHCID 86711759HCID 8671175952%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2,4,6-trichloro-pyrimidin-5-ol (400 mg, 2.01 mmol) and 2-tert-butyl oxirane (3 mL) was heated at 100° C. for 3 hours before being cooled and concentrated in vacuo. The resultant residue was triturated in hot methanol and the insoluble material removed. The filtrate was concentrated in vacuo and the resultant residue was purified by column chromatography (SiO2, 0-15% ethyl acetate in cyclohexane) to give 3,3-Dimethyl-1-(2,4,6-trichloro-pyrimidin-5-yloxy)-butan-2-ol as a white solid (275 mg, 52%). 1H NMR (400 MHz, CDCl3): δ 4.28 (1H, dd, J=9.38, 2.19 Hz), 4.00 (1H, t, J=9.19 Hz), 3.76-3.69 (1H, m), 2.53 (1H, d, J=3.48 Hz), 0.95 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346817B2
Source datasetuspto-grants-2016_05
ORD IDord-2d53566aaa9845d286990760446641f1
Source noteuspto-grants-2016_05