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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246701Generated: November 1, 2026

Benzyl chloroformate → HCID 68719246, compound

https://huagongshe.com/reaction/2246701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
Reactant[(2R)-3-amino-2-hydroxypropyl]-(cyclohexylmethyl)phosphinic acidHCID 5310935—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 68719246HCID 6871924693.3%

Reaction Steps

To a mixture of ((R)-3-amino-2-hydroxy-propyl)-cyclohexylmethyl-phosphinic acid (7.05 g, 30 mmol) and potassium carbonate (12.42 g, 90 mmol) in water (90 mL) and THF (30 mL) was added benzyl chloroformate (7.65 g, 45 mmol). After stirring for 3 h at room temperature, the reaction mixture was diluted with ethyl acetate (150 mL) and 2N HCl (90 mL). After stirring vigorously for 10 min the aqueous layer was removed and the organic layer was diluted with heptane (200 mL). The resulting white precipitate was collected to yield ((R)-3-benzyloxycarbonylamino-2-hydroxy-propyl)-cyclohexylmethyl-phosphinic acid (10.5 g, 28 mmol). 1H NMR (CDCl3, 300 MHz): δ 7.32 (m, 5H), 5.45 (br s, 1H), 5.10 (s, 2H), 4.2 (m, 1H), 3.4 (dd, 1H), 3.20 (dd, 1H), 2.01-1.55 (m, 10H), 1.40-0.95 (m, 5H). 31P NMR (CDCl3, 300 MHz): δ 57.3. LC/MS m/z: [M+H]+=370.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687540B2
Source datasetuspto-grants-2010_03
ORD IDord-bbdb7b81cb6b41e896824edb573535bc
Source noteuspto-grants-2010_03