Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 178455454 | HCID 178455454 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178455455 | HCID 178455455 | 106.1% |
Reaction Steps
To an ice-cooled solution of 27.6 g (107 mmol) of trans-[4-(tert-butyl-dimethyl-silanyloxymethyl)-cyclohexyl]-methanol and 9.99 mL (128 mmol, 1.2 eq) of methanesulfonyl chloride in 350 mL of CH2Cl2 were added under stirring at 0-10° C. 29.6 mL (213 mmol, 2 eq) of Et3N within 20 min. The reaction mixture was then stirred at RT for 1 h. It was then partitioned between CH2Cl2, 1M HCl and water. The CH2Cl2-phase was dried over MgSO4 and concentrated to yield 38.2 g of crude trans-methanesulfonic acid 4-(tert-butyl-dimethyl-silanyloxymethyl)-cyclohexylmethyl ester as colorless viscous oil, MS: 354 (M+NH4+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442791B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-c221c22bc1304c25a6ab1f0b13a03ed1 |
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| Source note | uspto-grants-2008_10 |
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