HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471118Generated: October 26, 2026
Triethylamine → Ethyl 2-(cyclobutanecarboxamido)-3-mercaptopropanoate
https://huagongshe.com/reaction/471118
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclobutanecarboxylic acid | HCID 19494 | — |
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | Ethyl 2-amino-3-mercaptopropanoate hydrochloride | HCID 6432754 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2-(cyclobutanecarboxamido)-3-mercaptopropanoate | HCID 57989145 | — |
Reaction Steps
Triethylamine (15 mL) was added to a suspension of cyclobutanecarboxylic acid (2.57 mL) and ethyl 2-amino-3-mercaptopropanoate hydrochloride (5 g) in DMF (40 mL). The resulting mixture was cooled in an ice bath and a solution of T3P (1.57M in THF, 20.6 mL) was added dropwise. The resulting mixture was allowed to warm to RT and stirred overnight. The reaction was quenched with saturated sodium bicarbonate solution (50 mL) and the layers separated. The aqueous phase was extracted with DCM (2×100 mL). The combined organic solutions were washed with brine (100 mL), dried over sodium sulphate, filtered and evaporated. The resulting white solid was purified by silica gel chromatography eluting with 4:1 to 1:1 isohexane:ethyl acetate gradient. The fractions containing product were combined and evaporated to give the subtitled compound as a clear oil. Yield 3.20 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629271B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-e27398f9294b4c79a7eb6d97f5dcfd91 |
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| Source note | uspto-grants-2014_01 |
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