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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731185Generated: October 26, 2026

Tributylphosphine → (R/S) Ethyl 2-(6-(2,3-dihydro-1H-inden-2-yloxy)-1,2,3,4-tetrahydronaphthalen-1-yl)acetate

https://huagongshe.com/reaction/731185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant2-IndanolHCID 77936—
ReactantDiamideHCID 5353800—
ReactantEthyl 2-(6-hydroxy-1,2,3,4-tetrahydronaphthalen-1-yl)acetateHCID 57835772—
SolventBenzeneHCID 241—
Product(R/S) Ethyl 2-(6-(2,3-dihydro-1H-inden-2-yloxy)-1,2,3,4-tetrahydronaphthalen-1-yl)acetateHCID 57835728—

Reaction Steps

Tributyl phosphine (137 mg, 0.68 mmol) and TMAD (122 mg, 0.68 mmol) were added successively to a dry benzene (10 mL) solution of 2-indanol (92 mg, 0.68 mmol) and ethyl 2-(6-hydroxy-1,2,3,4-tetrahydronaphthalen-1-yl)acetate 52.5 (160 mg, 0.68 mmol) with stirring under a nitrogen atmosphere. The reaction mixture was stirred at room temperature for 2 days. The product was isolated by silica gel column chromatography after filtration and evaporation of the solvent in vacuo. (R/S)-Ethyl 2-(6-(2,3-dihydro-1H-inden-2-yloxy)-1,2,3,4-tetrahydronaphthalen-1-yl)acetate (52) was obtained as a colorless oil (85 mg, 35%). LC-MS ESI (pos.) m/e: 351 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582803B2
Source datasetuspto-grants-2009_09
ORD IDord-21c5694febe5434c96d24875121e642d
Source noteuspto-grants-2009_09