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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682330Generated: November 3, 2026

Benzyl Alcohol → HCID 67918807, compound

https://huagongshe.com/reaction/1682330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantBromotrimethylsilaneHCID 76113—
ReactantHCID 86745101HCID 86745101—
SolventDichloromethaneHCID 6344—
ProductHCID 67918807HCID 67918807—

Reaction Steps

23 ml (178 mmols) of trimethylsilyl bromide are added dropwise at room temperature to a solution of 18.3 g (44.5 mmols) of benzyl E-2-formylamino-4-methyl-5-diisopropylphosphono-3-pentenoate in 73 ml of dichloromethane. After 20 hours at room temperature 46 ml of benzyl alcohol are added dropwise, and the reaction mixture is allowed to stand for additional 20 hours at room temperature. The dichloromethane is distilled off, first 40 ml of ethanol and then dropwise 40 ml of propylene oxide in 40 ml of ethanol are added. The crystalline precipitate formed is filtered off, triturated with 200 ml of water and filtrated off again. Benzyl E-2-amino-4-methyl-5-phosphono-pentenoate of m.p. 196°-197° (decomp.) is thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05175344
Source datasetuspto-grants-1992_12
ORD IDord-07963610950c41babc9d8c66bc89c980
Source noteuspto-grants-1992_12