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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 5-Bromo-1,2,3,4-tetrahydronaphthalen-1-one | HCID 10889572 | — |
| Reactant | 5-Oxo-5,6,7,8-tetrahydronaphthalene-1-carbonitrile | HCID 10931873 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(Methoxymethylene)-5,6,7,8-tetrahydronaphthalene-1-carbonitrile | HCID 117599331 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08999990B2 |
|---|
| Source dataset | uspto-grants-2015_04 |
|---|
| ORD ID | ord-7387ed66835d488fab7a5a04e3437edb |
|---|
| Source note | uspto-grants-2015_04 |
|---|