HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42545Generated: October 29, 2026
Hydrochloric Acid → HCID 57889538, compound
https://huagongshe.com/reaction/42545
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Ethyl 3-(2-(benzyloxymethyl)-2H-tetrazol-5-yl)benzoate | HCID 57888757 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57889538 | HCID 57889538 | — |
Reaction Steps
A solution of ethyl 3-(2-(benzyloxymethyl)-2H-tetrazol-5-yl)benzoate (653 mg, 1.93 mmol) in THF (10 mL) was treated with a 0.5 M aqueous lithium hydroxide solution (5.8 mL, 2.9 mmol), and the reaction was stirred for about 16 hours. After this time, analysis by LC/MS indicated that the reaction had not gone to completion. As such, the mixture was treated with additional 0.5 M aqueous lithium hydroxide solution (1 mL, 0.5 mmol), and the reaction was stirred for an additional 6 hours. After this time, the THF was removed under reduced pressure, and the aqueous solution was treated with 1 N HCl (3.5 mL, 3.5 mmol). The resulting mixture was extracted 3× with ethyl acetate, and the combined organic phases were dried over sodium sulfate and concentrated in vacuo to yield 3-(2-(benzyloxymethyl)-2H-tetrazol-5-yl)benzoic acid as a colorless powder, which was used as-is in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536198B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-519e54179de64202a598a0221c3e3d65 |
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| Source note | uspto-grants-2013_09 |
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