HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420249Generated: October 28, 2026
Acetone → Methyl 3-Azidomethyl-2-thienyl Ketone
https://huagongshe.com/reaction/2420249
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 1-[3-(Bromomethyl)thiophen-2-yl]ethan-1-one | HCID 21701274 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 3-Azidomethyl-2-thienyl Ketone | HCID 20381562 | — |
Reaction Steps
To a solution of methyl 3-bromomethyl-2-thienyl ketone (5 g., 0.023 mole) in 42 ml. of acetone and 4 ml. of water was added sodium azide (1.56 g., 0.024 mole) with caution (exothermic!). The resulting solution was stirred at room temperature for 2.5 hours, the acetone evaporated, the residue diluted with water and extracted with diethyl ether. The combined extracts were washed with water, saturated sodium bicarbonate solution and saturated sodium chloride solution, dried over magnesium sulfate and the dried extracts evaporated to dryness to obtain 4.0 g. (97%) of yellow oil. 1H--NMR (CDCl3), ppm. (δ): 7.5 (d, J=5, aromatic-H), 7.2 (d, J=5, aromatic-H), 4.75 (s, CH2N3), 2.5 (s, CH3); IR spectrum (film, cm.-1 : 3100, 2100 (N3), 1660, 1525 and 1420.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04110342 |
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| Source dataset | uspto-grants-1978_08 |
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| ORD ID | ord-1b88bccd4c9847f48245b472a7e1d562 |
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| Source note | uspto-grants-1978_08 |
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