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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207141Generated: November 1, 2026

Sulfuric Acid → HCID 67462821, compound

https://huagongshe.com/reaction/2207141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactanttert-Butyl acetateHCID 10908—
ReactantFmoc-D-Ser(Bzl)-OHHCID 7019719—
SolventDichloromethaneHCID 6344—
ProductHCID 67462821HCID 6746282177%

Reaction Steps

N-[(9H-Fluoren-9-yl)methoxycarbonyl]-O-(benzyl)-D-serine (0.710 g, 1.70 mmole) in dichloromethane (8 mL) was treated with t-butyl acetate (3 mL) and concentrated sulfuric acid (40 μL) in a sealed flask at 0° C. Upon completion (TLC), the reaction was quenched with of dichloromethane (10 mL) and saturated aqueous potassium bicarbonate (15 mL). The organic layer was washed with distilled water, and evaporated. The resulting residue was purified by flash column chromatography (98:2 dichloromethane/methanol) to yield the title compound as a colorless oil (0.292 g, 77%); 1H NMR (CDCl3) δ 1.44 (s, 9H); 3.68 (dd, J=2.9 Hz, J=9.3 Hz, 1H); 3.87 (dd, J=2.9 Hz, J=9.3 Hz, 1H); 4.22 (t, J=7.1 Hz, 1H); 4.30-4.60 (m, 5H); 5.64-5.67 (m, 1H); 7.25-7.39 (m, 9H); 7.58-7.61 (m, 2H); 7.73-7.76 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376424B2
Source datasetuspto-grants-2016_06
ORD IDord-0fd8ccaf45c04a32ab4bb4e6e258e7a4
Source noteuspto-grants-2016_06