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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286998Generated: October 31, 2026

Triethylamine → HCID 178458014, compound

https://huagongshe.com/reaction/2286998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
ReactantHCID 178458047HCID 178458047—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178458014HCID 17845801485%

Reaction Steps

To a solution of 1-[1-(aminomethyl)ethyl]-1H-tetrazole-5-thiol hydrochloride (17 g) and triethylamine (19.33 g) in 50% aqueous dioxane (80 ml) was added a solution of 2-t-butoxycarbonyloxyimino-2-phenylacetonitrile (21.4 g) in dioxane (50 ml) under cooling in an ice bath. The mixture was stirred for 1.5 hours at ambient temperature and concentrated to third volume. The aqueous solution was washed with diethyl ether and the washings were reextracted with aqueous solution of potassium carbonate. The two aqueous solutions were combined, washed with diethyl ether and mixed with ethyl acetate. The mixture was acidified with 10% hydrochloric acid and the organic layer was separated out. The solution was dried over magnesium sulfate and evaporated to dryness. The residue was triturated with n-hexane to give 1-[1-{(N-t-butoxycarbonylamino)methyl}ethyl]-1H-tetrazole-5-thiol (19.15 g), mp 156° to 158° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04268509
Source datasetuspto-grants-1981_05
ORD IDord-dad8053dde8244a7b97c3844f65f9657
Source noteuspto-grants-1981_05