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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701907Generated: October 31, 2026

Water → HCID 13720667, compound

https://huagongshe.com/reaction/1701907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHexamethylphosphoramideHCID 12679—
ReactantHCID 20505173HCID 20505173—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13720667HCID 1372066745.4%

Reaction Conditions

Temperature-40 °C

Reaction Steps

A solution of pyridazin-3-ylmethyl 3-chloropropyl sulphide (28.2 g) in anhydrous tetrahydrofuran (35 cc) is added dropwise, in the course of 15 minutes and whilst keeping the temperature below -20° C., to a solution of potassium tert.-butoxide (24 g) in a mixture of anhydrous hexamethylphosphorotriamide (35 cc) and anhydrous tetrahydrofuran (190 cc). The reaction mixture is subsequently stirred for 1 hour 30 minutes at -40° C. and is then run, at 0° C., into a mixture of distilled water (500 cc) and diethyl ether (500 cc). After decantation, the aqueous phase is extracted with diethyl ether (250 cc). The ether extracts are combined, washed three times with distilled water (1500 cc in total), dried over anhydrous sodium sulphate and filtered, and the filtrate is concentrated to dryness under reduced pressure (20 mm Hg; 2.7 kPa) at 30° C. 2-(Pyridazin-3-yl)-tetrahydrothiophen (10.5 g) is thus obtained in the form of a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04379154
Source datasetuspto-grants-1983_04
ORD IDord-dca1eeb0e48a46d7b6a5014253e628bf
Source noteuspto-grants-1983_04