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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092924Generated: November 3, 2026

Dichloromethane → HCID 86632036, compound

https://huagongshe.com/reaction/1092924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantBENZYL 3-HYDROXYPHENYLACETATEHCID 7016416—
ReactantHCID 86632037HCID 86632037—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 86632036HCID 8663203631%

Reaction Conditions

Temperature0 °C

Reaction Steps

Benzyl 3-hydroxyphenylacetate 0.88 g (3.60 mmol) was added to 30 mL of a dry dichloromethane solution containing 3.60 mmol of benzyl 2-(N-benzyloxycarbonylamino)-4-[chloro(methyl)phosphono]butanoate obtained in the same manner as Example 1. After the solution was cooled to 0° C., 0.51 mL (3.60 mmol) of triethylamine was added and stirred at 0° C. for 15 minutes. Thereafter, the temperature was increased and reaction was carried out at 34° C. for 45 minutes. After the completion of the reaction was confirmed by TLC (EtOAc/hexane=1:1), the reaction mixture was vacuum-concentrated and the residue was dissolved in 30 mL of ethyl acetate and the insoluble salt was removed by filtration. The filtrate was vacuum-concentrated, and the crude product was purified by flash column chromatography on neutral silica gel 60 N using a solvent mixture of ethyl acetate and hexane at 4:3 to obtain benzyl 2-(N-benzyloxycarbonylamino)-4-{[3-(benzyloxycarbonylmethyl)phenyl] (methyl)phosphono}butanoate as a colorless oily substance (0.72 g, yield 31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129557B2
Source datasetuspto-grants-2012_03
ORD IDord-f155f80994c64f11afb9f2bb6a405bfd
Source noteuspto-grants-2012_03