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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386166Generated: October 29, 2026

Triisopropyl phosphite → Diisopropyl phosphite

https://huagongshe.com/reaction/2386166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl phosphiteHCID 8304—
ReactantAcetic acid 2-chloromethoxy-ethyl esterHCID 10034810—
ProductDiisopropyl phosphiteHCID 307247%

Reaction Conditions

Temperature125 °C

Reaction Steps

A 500 mL three-neck flask was charged with the crude chloromethylether 1 (317 g, 2.00 mol). Triisopropylphosphite (494 mL) was added dropwise through an additional funnel while heating in a 125° C. oil bath and stirring vigorously. Collect 2-chloropropane distillate via short-path head in a dry ice cooled receiver, argon blanket, collected 140 g distillate (theoretical 157 g). Phosphite blanched reaction to yellow, continue heating another 2 h at 125° C. oil bath, then arrange for vacuum distillation using a vacuum pump. Distilled a yellow front cut (140 g, head to 135° C., bottom to 190° C.), then changed to clean receiver. Main fraction was collected at head temperature of 178-187° C. (mostly 185-187° C.) with vacuum unknown at bath temperature of 222-228° C. 258 g of the product 2 was given (47% yield from 1,3-dioxolane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268802B2
Source datasetuspto-grants-2012_09
ORD IDord-5c8954c3cdf74bf7b9dc4b1a8ecf3392
Source noteuspto-grants-2012_09