Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 178471406 | HCID 178471406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178471407 | HCID 178471407 | — |
Reaction Steps
2-(Ethoxy)(hydroxymethyl)phosphinoylmethyl-4-methylpentanoic acid ethyl ester (5 g) was dissolved in 20 mL of CH2Cl2 and cooled to −20° C. (in duplicate). Methanesulfonyl chloride (1.5 mL) and triethylamine (3.0 mL) were added to solution dropwise. After 15 minutes the bath was removed and the reaction left at room temperature for 3% hours. Each solution was then washed with 10 mL cold 2% HCl, 10 mL NaHCO3 (sat), mL brine, dried with MgSO4, filtered and evaporated to yield 12.8 g (combined yield) of 2-(ethoxy)(methane-sulfonyloxymethyl)phosphinoylmethyl-4-methylpentanoic acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06579890B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-e66056a4b8ef4cd7b3339a4e185468dc |
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| Source note | uspto-grants-2003_06 |
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