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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555383Generated: October 31, 2026

Triphenylphosphine → HCID 66629762, compound

https://huagongshe.com/reaction/555383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantEthyl 4-hydroxycyclohexanecarboxylateHCID 86973—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantHCID 66630625HCID 66630625—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66629762HCID 6662976232%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of N-adamantan-2-yl-4-hydroxy-benzamide (6 g, 22.11 mmol) in dry THF (100 mL) was added triphenyl phosphine (8.7 g, 33.17 mmol) and 4-hydroxy cyclo-hexane carboxylic acid ethyl ester (4.57 g, 26.53 mmol). The reaction mixture was cooled to 0° C. and DEAD (5.22 mL, 33.17 mmol) was added dropwise from an addition funnel over a period of 30 min. The reaction was gradually brought to room temperature and stirring continued for 48 hrs. The solvent was removed under vacuum and ether (100 mL) was added and cooled to 0° C. The solid formed was filtered off and the clear filtrate concentrated and purified by column chromatography (Gyan-flash). Desired fractions were collected and the solvent evaporated. The residue was crystallised from diethyl ether and filtered off affording 3 g (32%) of 4-[4-(adamantan-2-ylcarbamoyl)-phenoxy]-cyclohexane carboxylic acid ethyl ester as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053447B2
Source datasetuspto-grants-2011_11
ORD IDord-be25847febdc45d8b7d9e026aba4c80e
Source noteuspto-grants-2011_11