HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443746Generated: October 29, 2026
Pyridine → Isopropyl (chlorosulfinyl)(phenyl)carbamate
https://huagongshe.com/reaction/443746
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Propham | HCID 24685 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Isopropyl (chlorosulfinyl)(phenyl)carbamate | HCID 12728807 | 61.1% |
Reaction Steps
Eighteen grams isopropyl phenylcarbamate (~0.1 mol) and 14.0 g thionyl chloride (0.12 mol) were dissolved in 50 ml dry tetrahydrofuran and protected from moisture by a calcium chloride tube. Eight grams pyridine (0.1 mol) were added dropwise while the mixture was stirring at a water bath temperature (15°-20° C.). After the addition of pyridine was completed, the mixture was stirred for 12 hours at room temperature. Pyridine hydrochloride was filtered and the solvent was removed under vacuum. The concentrated residue was diluted with hexane and filtered. The hexane was removed under vacuum and the residue was distilled, giving 16.0 g of product distilling at 113-115/0.08 mm. NMR spectrum of the product in chloroform-d-TMS gave the following absorptions: δ7.6-7.2 (m, 5H, phenyl protons), δ5.5-4.9 (m, 1H, CH) and δ1.4-1.3 (d, 6H, C(CH3)2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04261897 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-bf312fb42f2541cb8fb0654ff628516a |
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| Source note | uspto-grants-1981_04 |
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