HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Homoserine → HCID 131729812, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Homoserine | HCID 12647 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 131729812 | HCID 131729812 | — |
Reaction Steps
To a suspension of L-homoserine (1 g, 8.4 mmol) in acetonitrile (10 ml) at 0° C. was added 1,8-diazabicyclo[5.4.0]undec-7-ene (1.32 ml, 8.8 mmol, 1.05 eq). tert-butyldimethylsilyl chloride (1.33 g, 8.8 mmol, 1.05 eq) was then added portionwise over 5 minutes and the reaction mixture allowed to warm to room temperature and stirred for 16 hours. A white precipitate formed, which was filtered off and washed with acetonitrile before drying under reduced pressure. The title compound was isolated as a white solid (1.8 g, 92% yield). 1H NMR (500 MHz, DMSO-d6), δ: 7.5 (1H, br s), 3.7 (1H, m), 3.35 (4H, br m), 1.95 (1H, m), 1.70 (1H, m), 0.9 (9H, s), 0.1 (6H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08217050B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-bf7cc01357864e808d7b9f158cf716ad |
| Source note | uspto-grants-2012_07 |