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HRID 2379169作成日:2026年10月25日

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

https://huagongshe.com/reaction/2379169

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 h., 50% aqueous HOAc was added and the mixture was stirred 10 min. and then extracted with Et2O (2x). 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, 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US05360815
出典データセットuspto-grants-1994_11
ORD IDord-4f201e79f89247afbe8108d2f96f8c54
出典メモuspto-grants-1994_11