Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 69987458 | HCID 69987458 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69985687 | HCID 69985687 | 66.3% |
Reaction Steps
Acetic acid 3-amino-4-(t-butyl-diphenyl-silanyloxy)-phenyl ester (3.5 g, 8.6 mmol) was dissolved in anhydrous dichloromethane (150 mL) and anhydrous N,N-diisoproplyamine (1.5 mL) added. The solution was cooled to −78° C. and methanesulfonyl chloride (1.08 g, 9.05 mmol) added. The solution was stirred for 30 minutes and allowed to come to room temperature. The solution was stirred overnight. The reaction mixture was washed with water. The organic solvent was dried over anhydrous magnesium sulfate. The solution was filtered and the solvent evaporated to dryness in vacuo to yield the title compound as a solid (2.8 g, 5.7 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06506901B2 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-957e6e82be1c4865bdaeb039a12ad63e |
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| Source note | uspto-grants-2003_01 |
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