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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638121Generated: October 28, 2026

Water → HCID 18801164, compound

https://huagongshe.com/reaction/1638121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethyl phosphonic dichlorideHCID 12671—
Reactant4-Bromobenzyl alcoholHCID 70119—
SolventDichloromethaneHCID 6344—
ProductHCID 18801164HCID 188011644.5%

Reaction Steps

A solution containing 4-bromobenzyl alcohol (49.4 g, 0.26 mol) and Et3N (39 mL, 0.28 mol) in CH2Cl2 (150 mL) was slowly added to a cold (0° C.) solution of methyl phosphonic dichloride (36.96 g, 0.28 mol) in 200 mL of CH2Cl2, under N2. When the reaction was substantially complete, as determined by HPLC, an additional 39 mL of Et3N was added, followed by 20 mL of H2O resulting in an exotherm up to 27° C., followed by an additional 30 mL of H2O. According to HPLC, the reaction mixture contained 55% of the compound of Preparation 6, 4.5% of the desired compound and 20% of the compound of Preparation 1A. The reaction mixture was transferred to a separatory funnel and washed with 1N HCl (2×150 mL). The organic layer was combined with 150 mL of 2N NaOH and 50 mL of H2O, stirred overnight to hydrolyze the compound of Preparation 6 to the desired compound and then separated. The aqueous layer was washed with CH2Cl2 (2×150 mL), acidified with 22 mL of 12N HCl and then extracted with CH2Cl2 (400 mL). The organic extract was dried over Na2SO4, filtered and then dried in vacuo to provide 53.74 g of a white solid which was suspended in EtOAc (110 mL), stirred vigorously for 3 h, isolated by filtration and then dried in vacuo (at 50° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06043341
Source datasetuspto-grants-2000_03
ORD IDord-ee6b5daf6dd645669e369d7fd9645a1d
Source noteuspto-grants-2000_03