Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474005Generated: October 30, 2026

Cyclohexanol → HCID 15956113, compound

https://huagongshe.com/reaction/1474005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanolHCID 7966—
ReactantTriphenylphosphineHCID 11776—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant2-Chloro-5-(thiazol-2-ylamino)phenolHCID 86096006—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15956113HCID 159561135%

Reaction Steps

Following the procedure general for O-alkylation, Method C, 2-chloro-5-(thiazol-2-ylamino)phenol (70 mg, 0.31 mmol), 1-cyclohexanol (34 μM, 0.32 mmol), Ph3P (84 mg, 0.32 mmol) were suspended in THF (0.1 mL). The reaction flask was lowered into a sonication bath and sonicated for several minutes giving a clear and highly viscous solution. While sonication, DEAD (0.063 mL, 0.32 mmol) was added slowly. The reaction mixture was stirred for 1 h. The title compound was obtained after purification by flash chromatography on silica gel (hexane:EtOAc 7/3) in 5% yield (5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018209B2
Source datasetuspto-grants-2015_04
ORD IDord-f44d642e5acc4774b4662965dc765cd7
Source noteuspto-grants-2015_04