Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | N-Boc-serinol | HCID 10631565 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Acetate | HCID 175 | — |
| Product | N-Boc-serinol | HCID 10631565 | — |
Reaction Steps
Methanesulfonyl chloride (130 mmol) was added at 5° C. to a stirred solution of boc-serinol (40 mol) and triethylamine (25 ml) in dichloromethane (100 ml). The mixture was stirred at 5° C. for 5 h and at 20° C. for 20 h. Dichloromethane (200 ml) was added and the mixture was washed with an aqueous solution of sodium hydrogen carbonate (50 mM), dried (Na2SO4) and concentrated to dryness under vacuum. Chromatography of the residue on silicagel (1.2 L) eluting with hexane/ethyl:acetate (50:50) gave bis-(methanesulfonic acid ester) of boc-serinol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318795B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-b1999b5c4a054b7ab5a60dbf65f4ed67 |
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| Source note | uspto-grants-2012_11 |
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