HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → HCID 15085407, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethanol, 2-[2-[2-(2-mercaptoethoxy)ethoxy]ethoxy]- | HCID 10465720 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethanol ethylacetate | HCID 21584252 | — |
| Product | HCID 15085407 | HCID 15085407 | 83% |
Reaction Steps
To 2-{2-[2-(2-mercapto-ethoxy)-ethoxy]-ethoxy}-ethanol (310 mg, 1.47 mmol) and trityl chloride (452 mg, 1.62 mmol, 1.1 eq.) in a round bottomed flask was added simultaneously triethylamine (2.1 ml, 10 eq.) and THF (25 ml) under argon. The initial red colour faded upon stirring at ambient temperature for 1 hour. The reaction was monitored by TLC, ethyl acetate/ethanol (1:1) and was completed after 6 hours. Thereafter methanol (6 ml) was added to consume excess trityl chloride and the mixture stirred for 5 minutes before evaporation of the solvents. The residue was purified by flash chromatography using 100% ethyl acetate to afford the product (550 mg, 83%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07368474B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-ca9e807440e34433a3ff48aa6802a408 |
| Source note | uspto-grants-2008_05 |