HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2R)-Oxiran-2-ylmethyl butanoate → HCID 53833784, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2R)-Oxiran-2-ylmethyl butanoate | HCID 2724536 | — |
| Reactant | Carbamic acid, [3-fluoro-4-(3-thiazolidinyl)phenyl]-, phenylmethyl ester | HCID 57053099 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | HCID 53833784 | HCID 53833784 | 78% |
Reaction Steps
Using the same general procedure as step 3 of example 1, 3-[2-fluoro-4-(benzyloxycarbonyl) aminophenyl]thiazolidine (692 mg, 2.24 mmol) was treated sequentially with n-butyllitium (1.5 mL, 2.40 mmol) and (R)-(-)-glycidylbutyrate (0.33 mL, 2.33 mmol) to provide 500 mg (78%) of the title compound. Recystallization from methylene chloride/hexane provided an analytical sample with a melting point of 96°97° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688792 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-73136a57c2334676b72620b113a3be28 |
| Source note | uspto-grants-1997_11 |