HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → HCID 18397091, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 18397089 | HCID 18397089 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18397091 | HCID 18397091 | 414.1% |
Reaction Steps
To 10 ml of a chloroform solution of 0.19 g (0.4 mmol) of the (R)1-trifluoromethyl-6-ethoxyhexyl 6-benzyloxy-3,4-dihydro-2-naphthalenecarboxylate obtained in the first step was added 0.1 ml (0.4 mmol) of iodotrimethylsilane in a nitrogen atmosphere with stirring, and the mixture was reacted at room temperature for two and a half hours with stirring. Then, 8 ml of methanol was added, and the mixture was rapidly concentrated at room temperature under reduced pressure. The concentrate was separated by column chromatography, to obtain 0.64 g of (R)1-trifluoromethyl-6-ethoxyhexyl 6-hydroxy-3,4-dihydro-2-naphthalenecarboxylate as a crude product. The 1H-NMR data of this compound are described below. 1H-NMR (CDCl3), δ (ppm)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06019911 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-f02ffdd1b851419385eb5f51eda019e2 |
| Source note | uspto-grants-2000_02 |