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HRID 21566作成日:2026年10月26日

Acetic Acid → 6-Benzyloxymethyl-2-methyl-5,6-dihydro-4H-pyran-4-one

https://huagongshe.com/reaction/21566

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Magnesium BromideHCID 82241—
反応物(Phenylmethoxy)acetaldehydeHCID 108989—
反応物1,3-Bis (trimethylsilyloxy)butadieneHCID 54494435—
溶媒TetrahydrofuranHCID 8028—
生成物6-Benzyloxymethyl-2-methyl-5,6-dihydro-4H-pyran-4-oneHCID 1993304260%

反応手順

A solution of 10.4 g of the aldehyde from Step 1 in 250 ml of THF was cooled to 0° C. and 1.0 eq of freshly prepared MgBr2 was added dropwise. The mixture was warmed to r.t. and 40.6 g of 1,3-bis(trimethylsilyloxy)-1,3-butadiene (Emde, et al., Synthesis p. 6 (1982)) was added. After 3.0 h, 50% aqueous HOAc was added and the mixture was stirred 10 min and then extracted with Et2O (2×). After the ether was evaporated, the resultant oil was taken back up in 300 ml of CH2Cl2 and 12 ml of TFA. After 3 hours, the solution was washed with H2O, saturated NaHCO3, and brine and finally dried over MgSO4. After flash chromatography, 9.5 g (60%) of the title compound was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05424320
出典データセットuspto-grants-1995_06
ORD IDord-4f1710eda3b94485a32923fad0a20b4b
出典メモuspto-grants-1995_06