Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | L-Alanine | HCID 5950 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 178462210 | HCID 178462210 | — |
Reaction Steps
Thionyl chloride (27 mL) was added drop-wise to a solution L-alanine (42) (6.83 g, 76.6 mmol) in benzyl alcohol (120 mL). After stirring at 0° C. for 2 h, the reaction mixture was warmed to room temperature and stirred for a further 24 h and then evaporated to dryness under reduced pressure. Trituration with diethyl ether, followed by filtration and evaporation under reduced pressure, provided the crude product 43 (3.5 g), which was used directly without further purification. LC-MS (M-Cl)+=180
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09370569B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-2535ce0fffd54aea840acbbc2e12a416 |
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| Source note | uspto-grants-2016_06 |
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