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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750183Generated: October 28, 2026

Water → Thioacetic acid S-((S)-2-tert-butoxycarbonylamino-4-methyl-pentyl)ester

https://huagongshe.com/reaction/1750183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttoluene-4-sulfonic acid (S)-2-tert-butoxycarbonylamino-4-methyl-pentyl esterHCID 14081313—
ReactantPotassium ethanethioateHCID 23670855—
SolventDimethylformamideHCID 6228—
ProductThioacetic acid S-((S)-2-tert-butoxycarbonylamino-4-methyl-pentyl)esterHCID 1418650790.4%

Reaction Steps

To 1.00 g of toluene-4-sulfonic acid (S)-2-tert-butoxycarbonylamino-4-methyl-pentyl ester in 10 ml DMF were added 308 mg of potassium thioacetate. After 24 h at room temperature, the reaction was poured unto water, the pH was then adjusted to 9 and the mixture was extracted with ethyl acetate twice. The combined organic phases were washed with brine until neutral, dried over sodium sulphate and concentrated in vacuo. 0.67 g (90%) of Thioacetic acid S—((S)-2-tert-butoxycarbonylamino-4-methyl-pentyl)ester were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156796B2
Source datasetuspto-grants-2015_10
ORD IDord-84e740c976254d55a9f91dade3e6d585
Source noteuspto-grants-2015_10