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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678659Generated: November 2, 2026

Triphenylphosphine → HCID 67131198, compound

https://huagongshe.com/reaction/1678659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
ReactantMethyl 4-hydroxy-3,5-dimethylbenzoateHCID 12389264—
ReactantHCID 67131197HCID 67131197—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67131198HCID 6713119827%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-[2-(4-chloro-phenyl)-2H-indazol-3-yl]-2-cyclohexyl-ethanol (20 mg, 56 umol) in THF (1 ml) was added 4-hydroxy-3,5-dimethyl-benzoic acid methyl ester (11 mg, 62 umol; CAS Reg. No. 34137-14-9) and tri-phenylphosphine (18 mg, 68 umol) at ambient temperature under an argon atmosphere. The mixture was cooled to 0° C., di-tert-butyl azodicarboxylate (16 mg, 68 umol) was added and the suspension was stirred for 14 h at ambient temperature. The solvent was removed under reduced pressure to give a solid which was purified by column chromatography (silica gel, iPrOAc/heptane) to obtain the title compound (8 mg, 15 umol; 27%) as colorless oil. MS: m/e=517.3 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008505B2
Source datasetuspto-grants-2011_08
ORD IDord-a54cd12794a440aaa6c31c1d9b2a1afd
Source noteuspto-grants-2011_08