HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912072Generated: October 31, 2026
Triethylethylenediamine → HCID 71114713, compound
https://huagongshe.com/reaction/1912072
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylethylenediamine | HCID 66040 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | Sodium hexamethyidisilazane | HCID 45051731 | — |
| Reactant | HCID 71114729 | HCID 71114729 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 71114713 | HCID 71114713 | — |
Reaction Steps
A solution of (R)-4-benzyl-3-(5-benzyloxypentanoyl)oxazolidin-2-one (132 g) in tetrahydrofuran (660 mL) was added dropwise to a mixture of sodium hexamethyldisilazane (1.9 M in tetrahydrofuran) (702 mL) and tetrahydrofuran (660 mL) at −78° C. The reaction temperature was rose to −40° C. To the mixture was added dropwise tert-butyl bromoacetate (85 mL) at −78° C. The reaction temperature was rose to −36° C. To the mixture was added dropwise N,N,N′-triethylethylenediamine (33 mL) at ice temperature. And then, to the mixture were added water (530 mL) and hexane (660 mL). The aqueous layer was removed, and the organic layer was washed with aqueous 20 w/v % citric acid (660 mL×3), water (660 mL), saturated aqueous sodium bicarbonate (660 mL) and brine (660 mL), then dried over magnesium sulfate. The magnesium sulfate was filtered off and the filtrate was concentrated in vacuo to give the title compound (196 g) as a crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08604069B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-7b99c2805d0145119d7d679cf144b258 |
|---|
| Source note | uspto-grants-2013_12 |
|---|