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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657705Generated: October 26, 2026

Triethylamine → N-t-butoxycarbonyl-p-hydroxymethylphenylglycine

https://huagongshe.com/reaction/1657705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCarbonazidic acid, 1,1-dimethylethyl esterHCID 61256—
Reactantp-HydroxymethylphenylglycineHCID 53754844—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductN-t-butoxycarbonyl-p-hydroxymethylphenylglycineHCID 2056472963%

Reaction Steps

To a solution of p-hydroxymethylphenylglycine (8.0 g, 0.044 mole) and triethylamine (8.8 g., 0.087 mole) in 160 ml water was added t-butoxycarbonyl azide (6.95 g., 0.049 mole) dissolved in 120 ml tetrahydrofuran. After stirring overnight at room temperature, the reaction mixture was washed twice with 200 ml. portions of ether. The aqueous layer was covered with ether and in an ice bath was acidified to pH 3-3.5 with 3N hydrochloric acid. The acidic solution was extracted three times with 200 ml portions of ether. The combined ether layers were washed with saturated sodium chloride solution, dried, and the ether evaporated under reduced pressure. The resulting oil was triturated with chloroform-hexane and the solid filtered off to give N-t-butoxycarbonyl-p-hydroxymethylphenylglycine (7.74 g, 63% yield), m.p. 139°-141.5° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03962230
Source datasetuspto-grants-1976_06
ORD IDord-f1ba90c094a647149677178782dbb37e
Source noteuspto-grants-1976_06