Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 23253892 | HCID 23253892 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57062055 | HCID 57062055 | — |
Reaction Steps
A solution of 3.9 g of 3-hexyn-1,6-diol mono-t-butyl-dimethylsilyl ether in 50 ml of methylene chloride was cooled to -20° C. and treated with 4.18 ml of triethyl amine and then 1.77 ml of methane sulfonyl chloride. After stirring 15 minutes at -20° C. the reaction mixture was diluted with water and extracted twice with 50 ml of methylene chloride. The organic layers were washed with brine, dried over sodium sulfate and evaported in vacuo to give the 3-hexyn-1,6-diol t-butyldimethylsilyl ether methyl sulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04515727 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-c53ad314eb8446d08c46165a390e3a15 |
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| Source note | uspto-grants-1985_05 |
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