HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(Benzyl-tert-butoxycarbonylmethyl-amino)-cyclohexanecarboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | 4-Benzylamino-cyclohexanecarboxylic acid tert-butyl ester | HCID 68724841 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Benzyl-tert-butoxycarbonylmethyl-amino)-cyclohexanecarboxylic acid tert-butyl ester | HCID 68725486 | 34.1% |
Reaction Steps
To a solution of 4-benzylamino-cyclohexanecarboxylic acid tert-butyl ester (630 mg, 2.180 mmol) in DMF (20 mL) is added t-butyl bromoacetate (1 mL, 6.856 mmol) and Cs2CO3 (1.0 g, 3.069 mmol). The mixture stirs for 2 h. Then H2O (50 mL) is added the mixture is extracted with EtOAc (2×100 mL), dried with sodium sulfate and concentrated. The resulting solid is purified by flash chromatography (gradient elution: 0-20% EtOAc/Hep) which affords 300 mg of 4-(benzyl-tert-butoxycarbonylmethyl-amino)-cyclohexanecarboxylic acid tert-butyl ester. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.24 (m, 5H), 1.38 (m, 18H), 1.86 (m, 4H), 2.09 (m, 1H), 3.14 (m, 2H), 3.71 (m, 2H), 7.29 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691756B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-7775c15d56d04f59b178d7fa0d4eac6b |
| Source note | uspto-grants-2014_04 |