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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173345Generated: October 30, 2026

Ethyl orthoformate → HCID 67517270, compound

https://huagongshe.com/reaction/2173345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantSodium AzideHCID 33557—
Reactant5-Amino-2,3-dihydro-1H-indene-1-carboxylic acidHCID 12318493—
SolventAcetic AcidHCID 176—
ProductHCID 67517270HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-337c63e64e2240abbbab462ab6d2463f
Source noteuspto-grants-2015_06