HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 2-(2-(Benzyloxy)ethoxy)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Butyl[2-(benzyloxy)ethoxy]acetate | HCID 131731128 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2-(Benzyloxy)ethoxy)acetic acid | HCID 21790136 | 95.1% |
Reaction Steps
To a stirred solution of ester 9 (2.66 g, 10 mmol) in dichloromethane (91 ml) was added TFA (9 ml) reaction mixture was stirred at room temperature for 2 hrs and mixture was concentrated. Obtained residue was diluted in water and basified with a NaOH 1N solution. This aqueous layer was extracted with ether then acidified and extracted twice with EtOAc. Combined organic layers were dried over MgSO4, filtered and concentrated to give acid 10 (2 g, 95%) as an oil, used for next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08624044B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-18f059ec4e394ed4a143aabcbc9df68f |
| Source note | uspto-grants-2014_01 |