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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantEthyl 3-bromo-4-oxopentanoateHCID 12933940—
ReactantSodium hydrogen sulfide hydrateHCID 53442613—
SolventWaterHCID 962—
ProductEthyl 3-mercapto-4-oxopentanoateHCID 8672413758.4%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150592B2
Source datasetuspto-grants-2015_10
ORD IDord-6b69e2e75d2542eb8b353965aa24e8ac
Source noteuspto-grants-2015_10