Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 93177-83-4 | HCID 14715186 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59324100 | HCID 59324100 | — |
Reaction Steps
27.3 gr (0.27 Mol) of 2-hydroxy-3-methoxy-propionitrile was dissolved dichloromethane (250 ml) and treated first with 56.4 ml (0.40 Mol) triethylamine keeping the temperature below −8° C., followed by dropwise addition of 23.1 ml (0.297 mol) methansulfonyl chloride keeping the temperature below +7° C. under cooling. After the exothermic reaction ceased the mixture was left to reach room-temperature. Water was stirred in, and the mixture was extracted with tert.-butylmethylether, washed with brine, dried and evaporated. To remove some polar side-products the crude liquid obtained was filtered through silica gel (eluent: cyclohexane/ethylacetate 1:1). Methanesulfonic acid 1-cyano-2-methoxy-ethyl ester of 89% purity (GC-MS) was obtained; 1H-NMR (CDCl3): 5.33, t, 1H, 3.81, d, 2H, 3.48, s, 3H, 3.21, s, 3H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110593B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-15dfb02a883f4738b88b0e9cded62a90 |
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| Source note | uspto-grants-2012_02 |
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