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HRID 405781作成日:2026年10月27日

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

https://huagongshe.com/reaction/405781

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 dichloromethane 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US08754071B2
出典データセットuspto-grants-2014_06
ORD IDord-3663cbdaaeb047ac91dd5d57d64ae722
出典メモuspto-grants-2014_06