HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetic Acid → HCID 44217165, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetic Acid | HCID 6227 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 44217648 | HCID 44217648 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 44217165 | HCID 44217165 | 57.8% |
Reaction Steps
A suspension containing [1-(4-fluorobenzyl)-1H-indazol-3-yl]methanol (6 g; 0.022 mol), bromoacetic acid (4 g; 0.03 mol) and 50% NaH (3 g; 0.066 mol) in THF (170 ml) was stirred at reflux for 72 hours. The reaction was then stopped by diluting with a suspension with water and ice (300 ml) and washing the aqueous phase with diethyl ether (3×150 ml). The aqueous phase was acidified with concentrated HCl. The solid thus formed was filtered off and purified by crystallization from isopropanol. 4 g of {[1-(4-fluorobenzyl)-1H-indazol-3-yl]methoxy}acetic acid were thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08835481B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-e37ccea55691465fb16e2e49f331aaa8 |
| Source note | uspto-grants-2014_09 |