HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Methyl (4R)-2-phenyl-1,3-thiazolidine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | L-Cysteine, methyl ester, hydrochloride | HCID 2733208 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl (4R)-2-phenyl-1,3-thiazolidine-4-carboxylate | HCID 14790915 | 88% |
Reaction Steps
To a suspension of L-cysteine methyl ester hydrochloride (1.717 g, 10 mmol) in tetrahydrofuran (5.0 mL) at room temperature under nitrogen was added benzaldehyde (1.02 mL, 10 mmol) followed by triethylamine (4.2 mL, 30 mmol). After stirring at room temperature for 3.5 hrs, the resulting mixture was filtered through a pad of silica gel eluting with EtOAc. Evaporation of the filtrate gave the title compound (1.95 g, 88%) as a colorless oil. TLC(EtOAc-hexane; 1:5) Rf=0.22.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157430B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-2194b992c06a4819a26c6ca96d373f8c |
| Source note | uspto-grants-2007_01 |