HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 21832179, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 2-Amino-1-(naphthalen-2-yl)ethan-1-ol | HCID 2735379 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-[4-(2-Oxopropoxy)benzyl]thiazolidine-2,4-dione | HCID 21832150 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21832179 | HCID 21832179 | — |
Reaction Steps
A procedure similar to that described in Preparation 10, below, was followed, but using 520 mg of 2-amino-1-(2-naphthyl)ethanol [prepared as described in Preparation 8], 650 mg of 5-[4-(2-oxopropoxy)benzyl]thiazolidine-2,4-dione [prepared as described in Preparation 9], 150 ml of benzene, 100 ml of absolute methanol and 1.25 g of sodium borohydride, to give the title compound in crude form. This crude product was then purified by column chromatography through silica gel, using a 5:1 by volume mixture of ethyl acetate and ethanol as the eluent, to give 490 mg of the title compound melting at between 115° C. and 145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05436257 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-71c05cdd02a34ea3a5c210a4b422dc44 |
| Source note | uspto-grants-1995_07 |