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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208645Generated: November 1, 2026

Hydrochloric Acid → HCID 22798347, compound

https://huagongshe.com/reaction/2208645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant2-PropanethiolHCID 6364—
ReactantSodium HydroxideHCID 14798—
ReactantN-tert-ButyloxycarbonylcysteineHCID 152319—
SolventEthanolHCID 702—
SolventOxolane--water (1/1)HCID 21881883—
ProductHCID 22798347HCID 2279834749.3%

Reaction Steps

Boc-L-Cys-OH (221 mg, 1.0 mmol) was dissolved in H2O/THF (50% v/v, 20 mL). To the solution was added 10 N sodium hydroxide aq. (1.2 mL, 12 mmol) and 2-propane thiol (929 uL, 10 mmol) at 0° C. Then, a solution of iodine in 95% EtOH was added dropwise until the color of the reaction system changed from colorless to brown. The mixture was stirred for 1 d with warming to room temperature. After removing THF under reduced pressure, reaction mixture was neutralized by 1 N HCl aq. until pH 2-3. The solution was extracted with EtOAc. The extract was washed with saturated aq. NaS2O4 and brine, and dried over MgSO4. Concentration under reduced pressure followed by flash chromatography over silica gel in EtOAc/Hexanes/AcOH (75:25:1) gave Boc-L-Csp-OH (145.7 mg, 49% yield): 1H NMR (360 MHz, CDCl3) δ 5.34 (s, 1H), 4.59 (br, s, 1H), 3.24-3.14 (m, 2H), 3.09-3.00 (m, 1H), 1.47 (s, 9H), 1.32-1.30 (dd, 6H); LRMS (ESI) m/z calcd for C11H22NO4S2 (M+H)+ 296.1. found 296.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376700B2
Source datasetuspto-grants-2016_06
ORD IDord-de012e366fe446708e931e2e5a737db1
Source noteuspto-grants-2016_06