HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158678Generated: November 3, 2026
Phosphate → [2-(4-Chloro-phenyl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/1158678
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphate | HCID 1061 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Fluorostyrene | HCID 67883 | — |
| Reactant | tert-Butyl carbamate | HCID 77922 | — |
| Reactant | Tert-Butyl hypochlorite | HCID 521297 | — |
| Catalyst | Potassium osmate(VI) dihydrate | HCID 53393272 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | [2-(4-Chloro-phenyl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester | HCID 16244250 | — |
Reaction Steps
To a stirred solution of carbamic acid tert-butyl ester (0.22 g) in acetonitrile (6 mL) was added in sequence at 0° C.: Sodium hydroxide (52 mg) in water (5 mL); after 2 minutes tert-butyl hypochlorite (139 mL); after 10 minutes potassium osmate(VI) dihydrate (9 mg) in water (1 mL); after 1 minute hydroquinine (anthraquinone-1,4-diyl)diether (26 mg) in acetonitrile (4 mL); after 3 minutes acetonitrile (6.7 mL) and phosphate buffer (3.3 mL, 0.5 M pH 7.65); after 5 minutes enough sodium biphosphate monohydrate to make pH=7.65; and finally 4-fluorostyrene. The reaction was quenched after stirring 3 hours at 25° C. with sodium sulfite (0.20 g) in water (2 mL) at 0° C. The phases were separated and the aqueous layer extracted with ethyl acetate (3×20 mL). The combined organic phases were washed with water
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812023B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-2af17e0e69b84991ae1437bf54fcdcac |
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| Source note | uspto-grants-2010_10 |
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