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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825344Generated: October 30, 2026

Diethyl Ether → HCID 101934792, compound

https://huagongshe.com/reaction/1825344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium 2-ethylhexanoateHCID 23672331—
ReactantHCID 131719867HCID 131719867—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 101934792HCID 10193479266.6%

Reaction Steps

Allyl (5R,6S)-6-[(R)-1-hydroxyethyl]-2-(1,5-diethylpyrazol-3-yl)carbapen-2-em-3-carboxylate (267 mg) in dichloromethane (2 ml) and ethyl acetate (2 ml) under argon were treated with sodium 2-ethylhexanoate (135 mg), followed by triphenylphosphine (17.5 mg), followed by tetrakis(triphenylphosphine)palladium(0) (28.3 mg) and the mixture was stirred for 45 min. Diethyl ether (100 ml) was then added, and after stirring for 30 minutes the mixture was centrifuged. The residual solid was washed with diethyl ether, and dried under a stream of argon. The solid was then taken up in a small amount of water and chromatographed on DIAION HP20SS resin eluting with water, followed by water/THF mixtures; 2%, 3%, 4% and 6% THF. Fractions were monitored by HPLC, and those containing the product were combined, reduced in volume and freeze-dried to give sodium (5R,6S)-6-[(R)-1-hydroxyethyl]-2-(1,5-diethylpyrazol-3-yl)carbapen-2-em-3-carboxylate as a solid (169 mg); υmax(KBr) 1752, 1593, 1433, 1382, 1288, and 1258 cm−1; λmax(H2O)/nm 298 (ε/dm3 mol−1 cm−1 9,031), 260 (sh) (ε 5853); δ(D2O) 1.19 (t, J 7.6 Hz), 1.27 (d, J ca. 6.8 Hz), 1.28 (d, J ca. 7.3 Hz) (together 9H), 2.60 (2H, q, J 7.5 Hz), 3.18 (2H, d, J 9.8 Hz), 3.46 (1H, dd, J 2.7 & 5.9 Hz), 4.05 (2H, q, J 7.2 Hz), 4.14-4,26 (2H, m), 6.48 (1H, s) ppm; [Found (electrospray ms) m/z 342 (MH)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045619B2
Source datasetuspto-grants-2006_05
ORD IDord-b201b43548b846e183559a313376392d
Source noteuspto-grants-2006_05