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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921965Generated: October 30, 2026

Trityl chloride → S-Trityl-L-Cysteine

https://huagongshe.com/reaction/1921965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantCysteine HydrochlorideHCID 60960—
ReactantSodium AcetateHCID 517045—
SolventDimethylformamideHCID 6228—
ProductS-Trityl-L-CysteineHCID 7604489%

Reaction Conditions

Temperature50 °C

Reaction Steps

L-Cysteine hydro-chloride (100 g, 0.634 mol) and trityl chloride (270 g, 0.969 mol) were stirred in DMF (400 mL) for 2 days at room temperature. A 10% sodium acetate solution (3.5 L) was then added dropwise and the white precipitate which formed was filtered and washed with distilled water. Afterward, the residue was stirred in acetone at 50° C. for 30 min after which it was cooled to 0° C. and filtered. The precipitate was washed with a little acetone and diethyl ether and dried in vacuo. S-Trityl-L-cysteine 1c (205 g, 89%) was obtained as a white powder. 1c: m.p. 192° C. (decomp); 1H NMR (300 MHz, DMSO-d6) δ 2.45 (dd, 1H, J=9 Hz, 12 Hz), 2.58 (dd, 1H, J=4.4 Hz, 12 Hz), 2.91 (m, 1H), 7.22-7.36 (m, 15H); 13C NMR (75.5 MHz, DMSO-d6): δ 33.8, 53.7, 66.4, 127.1, 127.8, 128.1, 128.4, 129.5, 144.5, 168.4. This material was directly used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173809B2
Source datasetuspto-grants-2012_05
ORD IDord-b4e07d4488eb4324a013feb577d91eba
Source noteuspto-grants-2012_05