Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090998Generated: October 27, 2026

Cyclohexanol → methyl 1-cyclohexyl-1H-indazole-3-carboxylate

https://huagongshe.com/reaction/2090998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanolHCID 7966—
ReactantTriphenylphosphineHCID 11776—
Reactantmethyl 1H-indazole-3-carboxylateHCID 657476—
ReactantDiethylazodicarboxylate tolueneHCID 66777355—
SolventTetrahydrofuranHCID 8028—
Productmethyl 1-cyclohexyl-1H-indazole-3-carboxylateHCID 6677814393%

Reaction Steps

To a mixture of methyl 1H-indazole-3-carboxylate (5.00 g), cyclohexanol (9.00 mL), triphenylphosphine (14.9 g) and tetrahydrofuran (100 mL) was added 40% diethyl azodicarboxylate toluene solution (25.6 mL), and the mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure, diethyl ether was added to the residue, and the mixture was stirred at 0° C. The precipitate was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:9, volume ratio) to give the title object compound (6.84 g, 93%) as a pale-red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-86826ed234a046229b5877ca30ddfe44
Source noteuspto-grants-2013_05