HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339142Generated: October 26, 2026
Dimethylformamide → Triethyl 4-methylpentane-1,2,2-tricarboxylate
https://huagongshe.com/reaction/339142
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Triethyl ethane-1,1,2-tricarboxylate | HCID 81961 | — |
| Solvent | Water | HCID 962 | — |
| Product | Triethyl 4-methylpentane-1,2,2-tricarboxylate | HCID 85546418 | — |
Reaction Steps
Sodium hydride (21 gram, 0.482 mole) was added to 200 ml dimethylformamide at 20° C. under nitrogen atmosphere. Then 80 grams (0.325 mole) of triethyl ethane-1,1,2-tricarboxylate (compound [3] made in example I) was added to the solution at a temperature of below 30° C. The reaction mixture was maintained at room temperature for 4 hours and 52 ml (0.482 mole) of isobutyl bromide (R2-X) was added drop wise after which the reaction mixture was stirred for another 20 hours at room temperature. When the reaction was complete 1 liter of cold water was added and the organic materials were extracted with dichloromethane (500 ml). The organic extracts were dried over sodium sulfate filtered and evaporated to give an oily substance, which was vacuum distilled to give 88 gram (89% of the theoretical maximum yield) triethyl 4-methylpentane-1,2,2-tricarboxylate, compound [4].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08889898B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-e0c06348e0fe416695c8adaa9fd04713 |
|---|
| Source note | uspto-grants-2014_11 |
|---|