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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941230Generated: November 2, 2026

Water → HCID 12475277, compound

https://huagongshe.com/reaction/1941230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCarbon DisulfideHCID 6348—
Reactant2'-HydroxyacetophenoneHCID 8375—
ReactantPotassium tert-butoxideHCID 23665647—
SolventBenzeneHCID 241—
ProductHCID 12475277HCID 1247527731%

Reaction Conditions

Temperature15 °C

Reaction Steps

Part A: Potassium t-butoxide (134 g, 1.2 mole) is covered with benzene (1 L) in a flame dried round bottom flask equipped with an overhead stirrer, addition funnel, thermometer, and a nitrogen inlet. This suspension is maintained at 15° C. A solution of o-hydroxyacetophenone (54.4 g, 48.1 ml, 0.4 mole) and carbon disulfide (30.4, 24 ml, 0.4 mole) in benzene (700 ml) is slowly added over 1.3 hours, applying an ice bath periodically in order to maintain the temperature 18° C. The slurry which forms is stirred at ambient temperature for one day. The reaction mixture is transferred to a separatory funnel containing water (4 L) and extracted with ether (4×250 ml) and EtOAc (3×250 ml). The aqueous layer is acidified with 10% H2SO4 (1 L) and stirred at ambient temperature overnight. The resulting solid is filtered off and dried in vacuo at 50° C. overnight to yield 22.07 g of 2-mercapto-4H-1-benzopyran-4-one. Mp 207°-8° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703075
Source datasetuspto-grants-1997_12
ORD IDord-778b2beb56b949129ae6133c55e4cc66
Source noteuspto-grants-1997_12