HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620804Generated: October 31, 2026
tert-Butyl mercaptan → Ethyl 5-(tert-butylsulfanyl)-2,2-dimethyl-4-oxopentanoate
https://huagongshe.com/reaction/1620804
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl mercaptan | HCID 6387 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 5-bromo-2,2-dimethyl-4-oxopentanoate | HCID 4090969 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Ethyl 5-(tert-butylsulfanyl)-2,2-dimethyl-4-oxopentanoate | HCID 3576811 | — |
Reaction Steps
To a reaction flask containing tetrahydrofuran (5.0-fold, V/W of starting material) was added 5-bromo-2,2-dimethyl-4-oxo-pentanoic acid ethyl ester (1.0 eq) under nitrogen. The mixture was cooled to a temperature of −5-0° C., and a solution of 2-methyl-2-propanethiol (1.2 eq) and triethylamine (1.25 eq) was added while maintaining the temperature below 0° C. The reaction was stirred at room temperature for 25 hours, and then hexane (3.0-fold, V/W of starting material) was slowly added. After agitating for 30 minutes, the solid material was removed by filtration and washed with 50% ethyl acetate/hexane solution. The filtrate was concentrated under reduced pressure to give the desired product, which was taken on to the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772495B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-3f005074dc9648be948a40463512051c |
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| Source note | uspto-grants-2014_07 |
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