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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274813Generated: October 28, 2026

Cyclohexyl isocyanate → HCID 70268737, compound

https://huagongshe.com/reaction/274813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl isocyanateHCID 18502—
ReactantHCID 18691618HCID 18691618—
SolventDichloromethaneHCID 6344—
ProductHCID 70268737HCID 70268737—

Reaction Steps

To a solution of [R-(R*,R*)] and [S-(R*,R*)]N-(2-amino-1,2-diphenylethyl)-N'-(4-nitrophenyl)urea (0.1 g, 0.27 mmol) in dichloromethane (10 mL) is added cyclohexyl isocyanate (0.03 g, 0.27 mmol) in one portion. The resulting mixture is stirred 1 hour at room temperature before filtering off the solid product. The product is suspended in hot diethyl ether, filtered, and dried in vacuo at 114° C. for 4 hours, mp 244°-245° C. IR (KBr): 3337, 2931, 1639, 1559, 1507, 1330, 700 cm-1 ; NMR (DMS-d6): 0.97-1.66 (m, 10H), 4.94 (m, 2H), 5.94 (d, 1H, J=7.5 Hz), 6.42 (d, 1H, J=7.5 Hz), 7.03-7.19 (m, 12H), 7.60 (d, 2H, J=9.2 Hz), 8.12 (d, 2H, J=9.2 Hz), 9.51 (s, 1H). Analysis calculated for C 28 H31N5O4 : C, 67.05; H, 6.23; N, 13.96. Found: C, 66.74; H, 6.22; N, 13.98.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389682
Source datasetuspto-grants-1995_02
ORD IDord-8072d8a4128e4a29a46bc6b852c264d7
Source noteuspto-grants-1995_02