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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657575Generated: November 1, 2026

Carbon Tetrachloride → HCID 9996696, compound

https://huagongshe.com/reaction/1657575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantDicyclohexylthioureaHCID 727200—
SolventDichloromethaneHCID 6344—
Solventtert-ButanolHCID 6386—
ProductHCID 9996696HCID 9996696—

Reaction Steps

A mixture of 2.4 gm. (0.01 mole) of N,N'-dicyclohexylthiourea, 3.15 gm. (0.012 mole) of triphenylphosphine, 1.55 gm. (0.01 mole) of carbon tetrachloride, and 1.0 gm. (0.01 mole) of triethylamine in 25 ml. of methylene chloride is stirred for 2.5 hr. at 40°-45°. The reaction mixture is concentrated and the residue extracted several times with hot Skellysolve B. The combined Skellysolve B extracts are cooled to room temperature, filtered and evaporated. The crude N,N'-dicyclohexylcarbodiimide is reacted with 5 ml. of morpholine in 10 ml of tert-butyl alcohol at reflux for 16 hours. The reaction mixture is evaporated, toluene added and concentrated to remove residual morpholine. The residue is partitioned between ether and 10% hydrochloric acid. The acid layer is basified with 20% sodium hydroxide solution, nitrogen bubbled through the solution to remove ether and cooled at 5°. The product is collected, 2.07 gm. (70%), m.p. 105°-107°. The HCl salt is prepared and recrystallized from acetonitrile-ether, m.p. 226°-227°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03961056
Source datasetuspto-grants-1976_06
ORD IDord-de28eb34e2894a0aab57759803beea8d
Source noteuspto-grants-1976_06