HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061065Generated: October 30, 2026
Tert-Butyl hypochlorite → HCID 44465318, compound
https://huagongshe.com/reaction/2061065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-Butyl hypochlorite | HCID 521297 | — |
| Reactant | HCID 86642702 | HCID 86642702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 44465318 | HCID 44465318 | 82.6% |
Reaction Steps
A solution of (4-amino-4-methylpentyl)trimethylphosphonium chloride hydrochloride (0.70 g, 2.82 mmol) in a mixture of methanol (20 mL) and water (10 mL) was cooled in an ice bath for 15 min. t-BuOCl (1.0 mL, 3.0 equiv, 8.5 mmol) was added in one portion via syringe to the colorless solution to give a deep yellow solution. The reaction mixture was stirred for 30 min at 0° C., then room temperature for 30 min. The methanol was removed under reduced pressure and the aqueous solution was purified via reverse phase chromatography on a Shimadzu Prep-LC utilizing water/methanol and 0.05% acetic acid as modifier. Fractions were collected using UV absorbance at 215 nm. Fractions were pooled frozen and lyophilized to give a pale yellow solid (0.654 g, 82.6%). 1H NMR (D2O, 400 MHz): δ 1.40 (s, 6H), 1.65-1.69 (m, 2H), 1.85-1.89 (d, J=14.4, 9H), 1.89-1.92 (m, 2H), 2.19-2.27 (m, 2H). LRMS (ESI+) for C9H21Cl2NP+ (244.1); Found: 244, 246 (M+, M2H+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278482B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-e3e2063839e24dceadcc58ac9c36def0 |
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| Source note | uspto-grants-2012_10 |
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