HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174458Generated: October 29, 2026
Hexamethyldisilazane → HCID 53248106, compound
https://huagongshe.com/reaction/2174458
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | HCID 53248105 | HCID 53248105 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 53248106 | HCID 53248106 | 75% |
Reaction Steps
(Z)-4-(3-carboxy-2-sulfopropylamino)-4-oxobut-2-enoic acid (450 mg, 1.60 mmol) in mixture of 10 ml of dry DMA and 50 ml of dry toluene was heated. After the temperature reached at 80° C., HMDS (hexamethyldisilazane, 1.80 ml, 8.63 mmol,) and ZnCl2 (3.2 ml, 1.0 M in diethyl ether) were added. The mixture was continued heated to 115˜125° C. and toluene was collected through Dean-Stark trap. The reaction mixture was fluxed at 120° C. for 6 h. During this period, 2×20 ml of dry toluene was added to keep the mixture volume around 8˜10 ml. Then the mixture was cooled, 1 ml of 1:10 HCl (conc)/CH3OH was added, evaporated, purified on SiO2 chromatography eluted with 1:5:0.01 CH3OH/CH2Cl2/HAc to afford 315 mg (75%) of the title product. 1H NMR (DMF-d7) 6.96 (s, 2H), 4.04 (dd, 1H, J=4.3, 13.8 Hz), 3.47 (m, 1H), 3.23 (dd, 1H, J=7.4, 14.7 Hz), 2.99 (dd, 1H, J=3.3, 16.8 Hz), 2.35 (dd, 1H, J=8.1, 16.9 Hz); 13C NMR 173.58, 172.18, 135.54, 54.61, 40.24, 32.43, ESI MS m/z−261.70 (M−H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09061995B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-efb291ef1cf849a69c7655a6e45fa330 |
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| Source note | uspto-grants-2015_06 |
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