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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466021Generated: October 30, 2026

Methoxymethyl-triphenylphosphonium chloride → 5-(Methoxymethylene)-5,6,7,8-tetrahydronaphthalene-1-carbonitrile

https://huagongshe.com/reaction/1466021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant5-Bromo-1,2,3,4-tetrahydronaphthalen-1-oneHCID 10889572—
Reactant5-Oxo-5,6,7,8-tetrahydronaphthalene-1-carbonitrileHCID 10931873—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-(Methoxymethylene)-5,6,7,8-tetrahydronaphthalene-1-carbonitrileHCID 117599331—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium bis(trimethylsilyl)amide (2 mL, 4 mmol, 2M in THF) was added to a stirred suspension of (methoxymethyl)triphenylphosphonium chloride (1.47 g, 4.3 mmol) in dry THF (20 mL) at 0° C. for 35 min and a solution of 5-Oxo-5,6,7,8-tetrahydronaphthalene-1-carbonitrile [prepared from 5-bromo-tetralone following the procedure described in PCT publication WO2004/071389A2, Intermediate 41](490 mg, 2.86 mmol) in THF (10 mL) added over 10 min. The mixture was stirred at 0° C. for 2 h and at room temperature for 1 h. Water was added and the mixture was partitioned between EtOAc and brine. The organic layer was dried and concentrated. The crude product was purified via preparative-TLC (PE:EtOAc=10:1) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999990B2
Source datasetuspto-grants-2015_04
ORD IDord-7387ed66835d488fab7a5a04e3437edb
Source noteuspto-grants-2015_04