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HRID 1045405作成日:2026年10月25日

Dimethyl Sulfoxide → 6-((benzyloxy)methyl)dihydro-2H-pyran-3(4H)-one

https://huagongshe.com/reaction/1045405

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物TriethylamineHCID 8471—
反応物Ammonium ChlorideHCID 25517—
反応物Oxalyl chlorideHCID 65578—
反応物6-(benzyloxymethyl)tetrahydro-2H-pyran-3-olHCID 58063706—
溶媒DichloromethaneHCID 6344—
生成物6-((benzyloxy)methyl)dihydro-2H-pyran-3(4H)-oneHCID 58063632—

反応条件

温度0 °C

反応手順

DMSO (1.15 mL, 16.2 mmol) was added to a stirred solution of oxalyl chloride (1 mL, 10.8 mmol) in dichloromethane (60 mL) at −78° C. After 10 minutes, a dichlotomethane solution of 6-(benzyloxymethyl)tetrahydro-2H-pyran-3-ol (14) (1.20 g, 5.40 mmol) was added. Stirring was continued for one hour then triethylamine (3.8 mL, 27 mmol) was added and slowly warmed to 0° C. The reaction was poured into saturated NH4Cl solution and the organic phase was washed with brine and dried (NaSO4). The residue was purified over silica gel using EtOAc and hexanes to give 6-(benzyloxymethyl)dihydro-2H-pyran-3(4H)-one (15).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08569283B2
出典データセットuspto-grants-2013_10
ORD IDord-c1f36ece35b8490a87ba36277688477d
出典メモuspto-grants-2013_10