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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900081Generated: November 4, 2026

Dimethylformamide → HCID 23371882, compound

https://huagongshe.com/reaction/1900081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHCID 23371856HCID 23371856—
CatalystHCID 178418476HCID 178418476—
ProductHCID 23371882HCID 23371882—

Reaction Steps

A suspension of 8.9 g of (RS)-3-(6-bromo-pyridin-3-yl)-5-methoxymethyl-oxazolidin-2-one, 6.5 g of 8-tributyl-stannyl-1,4-dioxaspiro[4,5]dec-7-ene and 1.4 g of bis(triphenylphosphine)palladium(II) dichloride in 40 ml of dimethylformamide was stirred at 85° under argon for 22 h. Then, the mixture was cooled, filtered over a Celite® pad, the filter cake was washed with a large amount of ethyl acetate and the organic phase was washed several times with semi-saturated sodium chloride solution. The aqueous phases were extracted with ethyl acetate, the organic phases were combined, concentrated to a volume of 250 ml, treated with 250 ml of saturated potassium fluoride solution and stirred for 30 minutes. The mixture was again filtered over a Celite® pad, the phases were separated and the aqueous phase was extracted with ethyl acetate. The organic phases were combined, dried with magnesium sulfate, concentrated and chromatographed over silica gel 60 with diethyl ether as the eluent. There were obtained 1.2 g of (RS)-3-[6-(1,4-dioxa-spiro[4,5]dec-7-en-8-yl)-pyridin-3-yl]-5-methoxymethyl-oxazolidin-2-one. 1H-nmr (CDCl3) ppm: 8.48 (s, 1H), 8.19 (d, 1H), 7.56 (d,1H), 6.50 (m, 1H), 4.79 (m, 1H), 4.12 (t, 1H), 4.02 (s, 4H), 3.98 (t, 1H), 3.64 (m, 2H), 3.44 (s, 3H), 2.80 (m, 2H), 2.52 (m, 2H), 1.96 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574055
Source datasetuspto-grants-1996_11
ORD IDord-69062331dba143ef828f6d84acaa3574
Source noteuspto-grants-1996_11