Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281029Generated: November 1, 2026

Glycine → HCID 4103388, compound

https://huagongshe.com/reaction/2281029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycineHCID 750—
ReactantPyridineHCID 1049—
ReactantEthyl isothiocyanateHCID 10966—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
ProductHCID 4103388HCID 410338890%

Reaction Conditions

Temperature40 °C

Reaction Steps

Glycine 36 (150 mg, 2.0 mmol) was dissolved in H2O (5.0 mL) and pyridine (5.0 mL) solution. The pH of the solution was adjusted to about 9.0 as shown by an indicator paper by the addition of 1M NaOH. The solution was heated to 40° C. and kept at that temperature during the reaction. Ethyl isothiocyanate 35 (0.263 mL, 3.0 mmol) was added with vigorous stirring. Small portions of 1M NaOH was added to keep the pH at about 9.0. The reaction was completed when the alkali consumption ceased (1 h). Pyridine and excess alkyl isothiocyanates were then removed by repeated extraction with equal volumes of benzene. Subsequently, an amount of conc. HCl (0.75 mL) was added and the mixture was refluxed for 2 h. The residue was extracted with ethyl acetate (2×150 mL). The organic layer was dried with brine and MgSO4, then concentrated in vacuo. Flash column chromatography on silica gel (hexane:ethyl acetate=2:1) of the residue afforded the desired product 37 in 90% yield (258 mg, pale yellow solid). 1H NMR (400 MHz, CDCl3): 6.88 (br, 1H), 4.06 (d, J=1.2 Hz, 2H), 3.89 (q, J=7.2 Hz, 2H), 1.25 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139575B2
Source datasetuspto-grants-2015_09
ORD IDord-0f69dac334204400bfcb27f08a587fe1
Source noteuspto-grants-2015_09