HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → Ethanethioic acid S-[tetrahydro-5-(hydroxymethyl)-3-thienyl]ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Ethanethioic acid S-[tetrahydro-5-[(phenylmethoxy)methyl]-3-thienyl]ester | HCID 54092544 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethanethioic acid S-[tetrahydro-5-(hydroxymethyl)-3-thienyl]ester | HCID 54469016 | — |
Reaction Steps
A 0° C. solution, under argon, of 0.123 g of product from Example 139 in 1.0 ml of dry chloroform is treated with 51.1 microliter of boron trifluoride etherate and 0.193 g of tetra n-butylammonium iodide. the reaction mixture is stirred at room temperature overnight and concentrated in vacuo. The residue is purified by chromatography (silica gel: 0-100% ethyl acetate/hexane) to give 0.079 g of the desired. product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05750735 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-b3d761b8773240b7918086a42f92c1c1 |
| Source note | uspto-grants-1998_05 |