Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 54574910 | HCID 54574910 | — |
| Product | HCID 54402299 | HCID 54402299 | — |
Reaction Steps
To a solution of the alcohol (Step 5) (230 mg, 0.47 mmol) in CHCl2 (2.5 mL) was added at -40° C. Et3N (100 μL, 0.717 mmol) and MsCl (45.0 μL, 0.574 mmo.). The resulting mixture was then warmed to 0° C. After a period of 10 min, a saturated solution of NaHCO3 was added. The mesylate was extracted with CH2C12, dried over Na2SO4, evaporated and co-distilled two times with toluene and used as such for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05472964 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-2d4410c0ad994e30a806dc25e70c9589 |
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| Source note | uspto-grants-1995_12 |
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