HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173345Generated: October 30, 2026
Ethyl orthoformate → HCID 67517270, compound
https://huagongshe.com/reaction/2173345
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 5-Amino-2,3-dihydro-1H-indene-1-carboxylic acid | HCID 12318493 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 67517270 | HCID 67517270 | — |
Reaction Steps
A solution of 5-aminoindane-1-carboxylic acid (2.95 g, 16.7 mmol), sodium azide (1.20 g, 18.3 mmol) and triethyl orthoformate (7.42 g, 50.1 mmol) in 20 mL of actic acid was heated to 100° C. for 3 hrs. After the reaction was completed, the mixture was cooled to ambient temperature. The solution was removed under vacuum and the residue was diluted with EtOAc, washed with brine, dried over anhydrous Na2SO4 and concentrated. The residue was purified with silica gel column chromatograph to give the crude product, then re-crystalization from DCM to yield 5-(1H-tetrazol-1-yl)indane-1-carboxylic acid. 1H-NMR (400 MHz, DMSO) δ ppm 10.0 (s, 1H), 7.75 (s, 1H), 7.66˜7.69 (m, 1H), 7.55 (d, J=8.1 Hz, 1H), 4.02˜4.06 (m, 1H), 2.88˜3.08 (m, 2H), 2.31 (q, J=8.1 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056859B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-337c63e64e2240abbbab462ab6d2463f |
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| Source note | uspto-grants-2015_06 |
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