HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (S)-methyl 2-(tert-butyldimethylsilyloxy)-4-mesylbutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (S)-methyl 2-(tert-butyldimethylsilyloxy)-4-hydroxybutanoate | HCID 11107713 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-methyl 2-(tert-butyldimethylsilyloxy)-4-mesylbutanoate | HCID 86636767 | — |
Reaction Steps
To a solution of (S)-methyl 2-(tert-butyldimethylsilyloxy)-4-hydroxybutanoate (91c, 3.9 g, 15.7 mmol) in anhydrous dichloromethane was added triethylamine, DMAP, and mesyl chloride. The reaction was allowed to stir for 1.5 h. The reaction was quenched with saturated aqueous NH4Cl. The aqueous phase was extracted with dichlormethane and the combine organic phases were washed with brine. The organic layer was dried over anhydrous sodium sulfate and the solvent removed in vacuo to yield (S)-methyl 2-(tert-butyldimethylsilyloxy)-4-mesylbutanoate (91d, 4.9 g, 15 mmol) as a yellow oil. [M+H] calc'd for C12H26O6SSi, 327. found, 327.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071766B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-489886fa2e4b416eb0f3dd0df1198fed |
| Source note | uspto-grants-2011_12 |