HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345960Generated: October 28, 2026
Phenyl Isothiocyanate → HCID 15027715, compound
https://huagongshe.com/reaction/345960
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl Isothiocyanate | HCID 7673 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | HCID 15027714 | HCID 15027714 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15027715 | HCID 15027715 | — |
Reaction Steps
To a solution of 1.81 g of methyl 3-cyanomethylthiophene-2-carboxylate and 1.62 g of phenyl isothiocyanate in 30 ml of tetrahydrofuran was added 480 mg of a 60% sodium hydride with stirring at 0° C. in a stream of nitrogen, and the mixture was stirred for 1 hour at room temperature. To the reaction mixture was added 1.14 ml of methyl bromoacetate at room temperature, and the mixture was stirred for 3 hours. To the reaction mixture was added 480 mg of a 60% sodium hydride, and the mixture was stirred overnight at room temperature. To the reaction mixture was added 100 ml of water, and precipitates were collected by a filtration. The precipitates were successively washed with water, benzene and n-hexane, and dried over to obtain 3.06 g of the desired product as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05059692 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-93d7189a34d64122a633fb28cbed543b |
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| Source note | uspto-grants-1991_10 |
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