HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796883Generated: November 2, 2026
Diisopropylcarbodiimide → HCID 178458024, compound
https://huagongshe.com/reaction/1796883
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | HCID 178506630 | HCID 178506630 | — |
| Product | HCID 178458024 | HCID 178458024 | 62.7% |
Reaction Steps
N,N′-diisopropylcarbodiimide (0.15 mL, 1.0 mmol) was added to the solution of LiAlHSeH (1.0 mmol) prepared as described above in Example One. The reaction mixture was stirred at 0° C. for one hour. The mixture was extracted with diethyl ether and washed with saturated NaCl solution. The organic layer was dried over sodium sulfate and evaporated to dryness. The residue was purified by flash chromatography on silica gel with dichloromethane:n-hexane (40:1) to give 0.13 grams (62%) N,N′-diisopropylselenourea as a white crystal; mp 142.6–148.2° C.; C7H16N2Se; IR (KBr) 1515, 1570, 3195, 3246 cm−1; 1H NMR (CDCl3) δ 1.19 (12H, d, J=6.4 Hz, CH3), 4.21 (2H, br s), 6.10 (2H, br s); 13C NMR (CDCl3) δ 22.4, 47.9,176.2; MS (EI): m/z=208 [M+]; HRMS: m/z=208.0478 calcd for C7H16N2Se, found 208.0503.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07033564B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-5ed905fe8de74dc98538b5d00f41163e |
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| Source note | uspto-grants-2006_04 |
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