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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973503Generated: October 30, 2026

Toluene → Benzyl (2R)-2-Benzyl-5-tert-butylmercapto-4-oxopentanoate

https://huagongshe.com/reaction/973503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactanttert-Butyl mercaptanHCID 6387—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantBenzyl (2R)-2-Benzyl-3-chloromethylcarbonylpropionateHCID 10449338—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductBenzyl (2R)-2-Benzyl-5-tert-butylmercapto-4-oxopentanoateHCID 1501811573%

Reaction Steps

To tert-butylmercaptan (0.11 ml) in dimethylformamide (5 ml) at 0° C. was added potassium bis(trimethylsilyl)amide in toluene (1.80 ml, 0.90 mmol, 0.5M) followed by the resultant compound from Example 34 (259.6 mg, 0.785 mmol) in dimethylformamide (3 ml). After 16 h at room temperature the mixture was diluted with ethyl acetate, washed with water and brine, then dried over Na2SO4 and evaporated. Chromatography of the residue on silica gel with 10% ethyl acetate in hexane afforded 219.6 mg (73%) of a colorless oil. 1H NMR (CDCl3) δ7.10-7.40 (m,10H), 5.07 (s,2H), 3.25 (s,2H), 3.18-3.29 (m,1H), 2.97-3.07 (m,2H), 2.78 (dd,1H), 2.71 (dd,1H), 1.25 (s,9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05063208
Source datasetuspto-grants-1991_11
ORD IDord-3b137e8635dc419084ff4b5fb4c72d5d
Source noteuspto-grants-1991_11