HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054921Generated: October 30, 2026
3-Methyl-2-butenoyl chloride → 3-Methylbut-2-enoyl isothiocyanate
https://huagongshe.com/reaction/1054921
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Methyl-2-butenoyl chloride | HCID 102394 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Catalyst | 3,6,9,12,15,18-Hexaoxanonadecan-1-ol | HCID 90207 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Methylbut-2-enoyl isothiocyanate | HCID 90017079 | 70.2% |
Reaction Steps
To a solution of potassium thiocyanate (10 g, 101 mmol, Eq: 1.00) and hexaethylene glycol monomethyl ether (896 mg, 830 μl, 3.02 mmol, Eq: 0.03) in dry dichloromethane (120 ml) was added dropwise at 0° C. a solution of 3-methylbut-2-enoyl chloride (12.0 g, 11.2 ml, 101 mmol, Eq: 1.00) in dry dichloromethane (20.0 ml) over 1 hour under argon atmosphere. After the addition was completed, the mixture (now light brown & turbid) was allowed to warm to 25° C. and was stirred for additional 3 hours. The mixture was filtrated, the filtrate was evaporated the residue was distilled under reduced pressure affording 3-methyl-but-2-enoyl isothiocyanate (9.989 g/70.2%) as a yellow liquid. GC-MS: m/ei=141 (M)/bp: 86° C./2 mbar
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394311B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-f8e3dfd69493417eb1f8b35517192db0 |
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| Source note | uspto-grants-2016_07 |
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