HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tosylmethyl isocyanide → HCID 71001888, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 86714576 | HCID 86714576 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 71001888 | HCID 71001888 | 80.3% |
Reaction Steps
Same procedure as that described in example 1, stage 1.4, starting from 8.7 g (32.7 mmol) of 4-methyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carbaldehyde, 6.7 g (34.3 mmol) of TOSMIC and 7.3 g (65 mmol) of potassium tert-butylate in solution in anhydrous DME (54 ml). 6.6 g of compound is obtained in the form of a yellow oil as 70/30 mixture of regioisomers tau and Pi.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09126972B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-4d3060c79fbf4c1c8ea55ca1f1661540 |
| Source note | uspto-grants-2015_09 |