Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-(+)-Cysteine | HCID 5862 | — |
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53800139 | HCID 53800139 | 81.9% |
Reaction Steps
109.5 g (0.9 mol) L-cysteine was placed in a 2000 ml flask, and dissolved with 1000 ml water, to which was added 24 ml of 1 mol/l NaOH solution. In an ice bath, 96 ml (1.8 mol) ethylene oxide was slowly added dropwise into the cysteine solution. After stirring 1 h, the ice bath was removed and the mixture was warmed to room temperature and further reacted for 1 h. The reaction product was extracted with 1000 ml anhydrous ethyl ether for four times, while collecting the aqueous layers. The aqueous layers were evaporated to dryness obtaining a yellow crystal product. The yellow crystal product was recrystallized with water:ethanol=85 ml:350 ml, filtered, washed with 2000 ml of 95% ethanol, and dried obtaining 121.8 g of a white crystal product, yield 74.3%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173643B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-ef4f3088d34e40608c1c099994cb4a89 |
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| Source note | uspto-grants-2012_05 |
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