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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968575Generated: October 31, 2026

Acetyl chloride → Isohexane ethyl acetate

https://huagongshe.com/reaction/1968575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantN-Boc-L-Leucine HydrateHCID 12373896—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductIsohexane ethyl acetateHCID 21882781—

Reaction Steps

Acetyl chloride (0.18 mL) was added dropwise to a solution of the dibromoalkene 9-2 (81.7 mg, 0.179 mmol) in MeOH (1.62 mL), chilled in an ice bath. The reaction mixture was stirred at RT overnight and then evaporated. Boc-Leu-OH—H2O (50 mg, 0.20 mmol), HATU (75 mg, 0.20 mmol), 1.8 mL DMF, and lastly, DIEA (125 μL, 0.72 mmol) were added. After stirring at RT for 5.5 h the mixture was concentrated in vacuo, and then partitioned between EtOAc and saturated aqueous NaHCO3. The organic phase was washed twice with saturated aqueous NaCl, dried (Na2SO4), and concentrated in vacuo. Flash chromatography (silica, 3/1 isohexane-EtOAc) gave compound 9-3 as a white solid (86.3 mg, 85% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426421B2
Source datasetuspto-grants-2013_04
ORD IDord-1f4a6ca396a648b4b168a361cecf01bf
Source noteuspto-grants-2013_04