HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → methyl (1R,2R)-2-(hydroxymethyl)cyclopropane-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | rac-(1R,2R)-2-(methoxycarbonyl)cyclopropane-1-carboxylic acid | HCID 12510972 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl (1R,2R)-2-(hydroxymethyl)cyclopropane-1-carboxylate | HCID 10931461 | — |
Reaction Steps
Add borane-methyl sulfide complex (177 mL, 0.354 mol), slowly, by means of a dropping funnel, to a stirring solution of trans-cyclopropane-1,2-dicarboxylic acid monomethyl ester (Example 3a) (25.5 g, 0.177 mol), trimethyl borate (60.3 mL, 0.531 mol) and tetrahydrofuran (150 mL) at 0° C. After complete addition, allow the reaction to come to ambient temperature and stir for 2 h more. Pour the reaction mixture into a stirring solution of 50% aqueous sodium chloride solution (1.5 L)-concentrated HCl (10 mL). Extract the mixture with ethyl acetate (EtOAc) (3 times), combine the extracts, dry (Na2SO4) and concentrate the solvent to obtain a colorless oil: 22.6 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07186724B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-d0f952f9aeea4e51aae9613756a290f2 |
| Source note | uspto-grants-2007_03 |