HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26996Generated: October 25, 2026
Triethylamine → 3-t-Butoxycarbonylaminomethyl-2-thienylacetic acid
https://huagongshe.com/reaction/26996
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Carbonazidic acid, 1,1-dimethylethyl ester | HCID 61256 | — |
| Reactant | 3-Aminomethyl-2-thienylacetic acid | HCID 15918143 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-t-Butoxycarbonylaminomethyl-2-thienylacetic acid | HCID 15918144 | 92% |
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 stirring. 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04151352 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-0ebb8843cadb45a19a8b61f469ed62b0 |
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| Source note | uspto-grants-1979_04 |
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