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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011607Generated: October 30, 2026

Methyl Acetate → HCID 67314184, compound

https://huagongshe.com/reaction/1011607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcetateHCID 6584—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 12995921HCID 12995921—
SolventEthyl AcetateHCID 8857—
ProductHCID 67314184HCID 6731418479%

Reaction Conditions

Temperature-78 °C

Reaction Steps

NaHMDS (428 mL, 1 M in hexane) was dissolved in THF (356 mL) and the resulting solution was cooled to −78° C. Methyl acetate (28.3 mL, 356 mmol) was added over 15 minutes and the reaction mixture was stirred at −78° C. for 1 h after which a solution (R,E)-N-(cyclopropylmethylene)-2-methylpropane-2-sulfinamide (26) (12.3 g, 71.3 mmol) in THF (50 mL) was added over 15 minutes. The reaction mixture was warmed to −20° C. and stirred at this temperature for 3 h after which HPLC indicated that the reaction was complete. The resulting solution was diluted with EtOAc (400 mL) and washed with sat. aq. NaHCO3 (200 mL). The organic phase was dried (Na2SO4), filtered, concentrated under vacuum and purified on a silica gel column (eluant hexane/EtOAc, 9/1 to 1/1 to give 16.3 g (79%) of (5S)-methyl 5-cyclopropyl-5-[(R)-1,1-dimethylethylsulfinamido]-3-oxopentanoate (27). Retention time (min)=1.397 method [1], MS (m/z) 290.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977368B2
Source datasetuspto-grants-2011_07
ORD IDord-ed44857a517c493b9f523009e1831295
Source noteuspto-grants-2011_07