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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266351Generated: November 2, 2026

Phenoxycarbonyl isothiocyanate → HCID 178491731, compound

https://huagongshe.com/reaction/1266351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenoxycarbonyl isothiocyanateHCID 12212046—
Reactant2-Cyano-thioacetimidic acid 4-methoxy-benzyl esterHCID 20577193—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
ProductHCID 178491731HCID 17849173173.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of of 2-cyano-thioacetimidic acid 4-methoxy-benzyl ester (42 g, 0.19 mol) in 191 mL of ethyl acetate at 0° C. was added phenoxycarbonylisothiocyanate (34 g, 0.19 mol), and the mixture was stirred at 0° C. for 24 hours. The mixture was diluted with ether and filtered. The solids were washed with ether, collected and dried in vacuo, affording 56 g (73%) of 2-cyano-3-mercapto-3-phenoxycarbonylamino-thioacrylimidic acid 4-methoxy-benzyl ester as a yellow solid. 1H NMR (400 MHz, CDCl3) δ 12.81 (s, 1H), 9.01 (s, 1H), 8.68 (s, 1H) 7.28-6.99 (m, 7H), 6.69 (d, 2H, J=8.8 Hz), 4.17 (s, 2H), 3.64 (s, 3H) ppm; MS (APCl, m/z): 400 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548526B2
Source datasetuspto-grants-2003_04
ORD IDord-00521b6192254c35b7a0202dcdec7846
Source noteuspto-grants-2003_04