HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748808Generated: October 30, 2026
Diethyl Ether → Ethyl 3-mercapto-4-oxopentanoate
https://huagongshe.com/reaction/1748808
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethyl 3-bromo-4-oxopentanoate | HCID 12933940 | — |
| Reactant | Sodium hydrogen sulfide hydrate | HCID 53442613 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 3-mercapto-4-oxopentanoate | HCID 86724137 | 58.4% |
Reaction Steps
A round bottom flask was charged with sodium hydrogensulfide hydrate (1.23 g, 16.9 mmol) in water (14.2 mL). The solution was cooled to about 0° C. followed by the addition of ethyl 3-bromo-4-oxopentanoate (3.79 g, 16.9 mmol) dropwise over about 30 min. The mixture was stirred at about 0° C. for about 3 h. To the reaction mixture was added Et2O (40 mL) and the reaction was warmed to ambient temperature. The crude product was partitioned between Et2O (15 mL) and water (15 mL). The layers were separated and the aqueous layer was back extracted with Et2O (10 mL). The combined organic layers were dried over MgSO4, filtered and concentrated under reduced pressure to afford ethyl 3-mercapto-4-oxopentanoate (1.74 g, 9.87 mmol, 58%, which was used without further purification). LC-MS (Table 1, Method g) Rt=2.24 min, m/z 177 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150592B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-6b69e2e75d2542eb8b353965aa24e8ac |
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| Source note | uspto-grants-2015_10 |
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