HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylcarbodiimide → HCID 131725937, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | O-(triphenylmethyl)hydroxylamine | HCID 3015602 | — |
| Reactant | 3-Methoxycarbonyl-hexanedioic acid 1-tert-butyl ester | HCID 86594384 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131725937 | HCID 131725937 | — |
Reaction Steps
To a solution of the compound of example 64 (1.10 g, 4.19 mmol) and HOBt (0.70 g, 5.03 mmol) in DMF (5 mL) were added O-trityl hydroxylamine (1.82 g, 6.28 mmol) and DIC (800 μL), respectively. The reaction mixture was stirred for 24 h at room temperature. The reaction mixture was partitioned between HCl (1N, excess) and ethyl acetate. The aqueous phase was extracted several times with ethyl acetate. The recombined organic layer was washed with brine, saturated sodium bicarbonate, and brine. The solvent was evaporated following drying over sodium sulfate, and the crude was flashed with 20–30% ethyl acetate in hexanes. 1H-NMR(CDCl3, 400 MH: 1.42(s, 9H); 1.58, 2.14, 2.47(3 m, 7H); 3.69(s, 3H); 7.34(m, 15H); 7.88(d, broad, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105539B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-ba55ca6f587b46729aa9409d8a9a32c0 |
| Source note | uspto-grants-2006_09 |