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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866706Generated: October 26, 2026

Triethylamine → 3-t-Butoxycarbonylaminomethyl-2-thienylacetic acid

https://huagongshe.com/reaction/866706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCarbonazidic acid, 1,1-dimethylethyl esterHCID 61256—
Reactant3-Aminomethyl-2-thienylacetic acidHCID 15918143—
SolventAcetoneHCID 180—
Product3-t-Butoxycarbonylaminomethyl-2-thienylacetic acidHCID 1591814492%

Reaction Steps

A mixture of 3-aminomethyl-2-thienylacetic acid 8 (3.1 g, 18 m. moles) and triethylamine (8 g. 80 m moles) in 50% aqueous acetone (80 ml) was added dropwise t-butoxycarbonyl azide (5.7 g, 40 m moles) over a period of 20 mins. at 0° C with vigorous sitrring. The reaction mixture was stirred overnight at room temperature and concentrated under reduced pressure. The concentrate was washed with ether (2 × 20 ml), adjusted to pH 2 with conc. HCl and extracted with ethyl acetate (2 × 50 ml). The ethyl acetate extracts were washed with saturated aqueous sodium chloride, dried over MgSO4, treated with charcoal and evaporated under reduced pressure. The residue was triturated with n-hexane and crystallized from n-hexane and benzene to give 4.5 g (92%) of colorless needles 9, melting at 62°-63° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04100346
Source datasetuspto-grants-1978_07
ORD IDord-93b608eb2e124e558b620c625fd4bba9
Source noteuspto-grants-1978_07