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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456959Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 15229884, compound

https://huagongshe.com/reaction/1456959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Hydroxymethyl-2,5,7,8-tetramethyl-chroman-6-olHCID 11746632—
SolventDichloromethaneHCID 6344—
ProductHCID 15229884HCID 1522988471.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution prepared by the sequential addition of oxalyl chloride (2.9 g, 23 mmol) and dimethyl sulfoxide (3.7 g, 47 mmol) to methylene chloride which had been cooled to -78° C. was allowed to stir for 12 minutes. A solution of 6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-benzo[1,2-b]pyran-2-yl methanol (4.0 g, 18 mmol) in 50 mL methylene chloride was then added dropwise to the reaction mixture. After stirring for 40 min., triethylamine (7.3 g, 72.6 mmol) was added dropwise over 5 min. The reaction mixture was stirred at -78° C. for 15 min and then at ambient temperature for 30 min. The reaction mixture was diluted with methylene chloride (100 mL). The resulting solution was washed (water 100 mL, brine 100 mL, water 100 mL), dried (magnesium sulfate), and concentrated under reduced pressure to give a yellow oil. The oil was chromatographed (SiO2, 200 g, ethyl acetate-hexane, 1:9) to give 6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-benzo[1,2-b]pyran-2-yl methanal as a white solid (3.0 g, 70% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05846988
Source datasetuspto-grants-1998_12
ORD IDord-28b946051d254dc287fe4d24c3494373
Source noteuspto-grants-1998_12