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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884403Generated: October 31, 2026

Acetyl chloride → Isohexane ethyl acetate

https://huagongshe.com/reaction/884403

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 (0.3 mL) was added dropwise to an ice-cooled solution of compound 7-3 (103.4 mg, 0.316 mmol) (see reference example 7) in methanol (2.9 mL). The solution was stirred at rt overnight, and then concentrated in vacuo, coevaporated twice with CH2Cl2, and dried under vacuum. Boc-L-leucine-H2O (96.2 mg, 0.386 mmol) and HATU (143 mg, 0.376 mmol) were added and the mixture was cooled in an ice bath. DMF (3.2 mL), followed by DIEA (220 μL, 1.26 mmol) were added. The resulting solution was stirred at rt for 6 h. The reaction mixture was concentrated in vacuo, redissolved in EtOAc (15 mL), and washed successively with saturated aqueous NaHCO3 (10 mL) and saturated aqueous NaCl (10 mL). The organic phase was dried (Na2SO4) and then concentrated in vacuo to give the crude material. Flash column chromatography (silica, 2/1 isohexane-EtOAc) gave compound 41 as white solids (127.8 mg, 92% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242119B2
Source datasetuspto-grants-2012_08
ORD IDord-7ba6074f47b24b50ae56ead38535e3e8
Source noteuspto-grants-2012_08