HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051112Generated: November 4, 2026
Lithium Hydroxide → 2-(3-((7-(3-Fluorophenyl)-1,2,3,4-tetrahydronaphthalen-1-yl)amino)phenoxy)acetic acid
https://huagongshe.com/reaction/1051112
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Isopropyl 2-(3-((7-(3-fluorophenyl)-1,2,3,4-tetrahydronaphthalen-1-yl)amino)phenoxy)acetate | HCID 118161548 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3-((7-(3-Fluorophenyl)-1,2,3,4-tetrahydronaphthalen-1-yl)amino)phenoxy)acetic acid | HCID 118161560 | 66% |
Reaction Steps
Aqueous lithium hydroxide (1 N, 1 mL, 1 mmol) was added to a solution of isopropyl 2-(3-((7-(3-fluorophenyl)-1,2,3,4-tetrahydronaphthalen-1-yl)amino)phenoxy)acetate (5 mg, 0.012 mmol) in THF (1 mL) in a scintillation vial. The vial was sealed and heated at 40° C. After 24 h, the reaction mixture was allowed to cool and the volatiles were concentrated in vacuo. The residue was acidified with hydrochloric acid (1 N, 1 mL), and extracted with ethyl acetate (3×2 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated to afford 3 mg (66%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388153B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-7ea164085da14b0eb9066a5ed4f47be2 |
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| Source note | uspto-grants-2016_07 |
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