HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 4-(Tert-butyldimethylsilyloxy)-2-ethylcyclopentanecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | HCID 67997857 | HCID 67997857 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | (1S,2R,4R)-4-(tert-butyldimethylsilyloxy)-2-ethylcyclopentanecarboxylic acid | HCID 67998141 | — |
| Product | 4-(Tert-butyldimethylsilyloxy)-2-ethylcyclopentanecarboxylic acid | HCID 58557083 | — |
Reaction Steps
To a scalemic mixture enriched in (1S,2R,4R)-2-ethyl-4-hydroxycyclopentanecarboxylic acid (2.56 g, 16.21 mmol) in DMF (10.81 mL) was added TBDMSCl (2.93 g, 19.45 mmol) and imidazole (2.76 g, 40.5 mmol). The reaction mixture was stirred at ambient temperature for about 2 days then extracted with pentane (3×25 mL). The combined pentane layers were washed with water (25 mL) and brine (25 mL), dried over anhydrous MgSO4, filtered and concd under reduced pressure. The residue was purified using silica gel chromatography eluting with 20-100% EtOAc in heptane give a scalemic mixture enriched in (1S,2R,4R)-4-(tert-butyldimethylsilyloxy)-2-ethylcyclopentanecarboxylic acid (1.13 g, 26%): LC/MS (Table 1, Method b) Rt=3.03 min; MS m/z: 273 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08426411B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-f3feaecbb5e041ea8c4855a137f93729 |
| Source note | uspto-grants-2013_04 |