HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579525Generated: October 25, 2026
Benzoyl chloride → 2-(Benzhydrylidene-amino)-2-benzoyl-hex-5-enoic acid tert-butyl ester
https://huagongshe.com/reaction/579525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 1,1-Dimethylethyl 2-[(diphenylmethylene)amino]-5-hexenoate | HCID 16066974 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Benzhydrylidene-amino)-2-benzoyl-hex-5-enoic acid tert-butyl ester | HCID 86663724 | 100% |
Reaction Steps
A solution of 2-(benzhydrylidene-amino)-hex-5-enoic acid tert-butyl ester (350 mg, 1 mmol) in THF (5 mL, 0.2 M) was cooled to −78° C. and treated with sodium bis(trimethylsilyl)amide (2.2 mL, 1.0 M, 2.2 equiv) drop wise over 5 min and stirred for 30 min. After adding benzoyl chloride (140 μl, 1.2 mmol, 1.2 eq), the reaction mixture was warmed up to room temperature and stirred for an additional 1.5 h. The solution was cooled to 0° C. and quenched with water (5 mL). The resulting solution was diluted with ethyl acetate and washed successively with water and saturated aqueous NaCl, dried over MgSO4, filtered and concentrated. Purification by MPLC (1-40% ethyl acetate in heptane gave 2-(benzhydrylidene-amino)-2-benzoyl-hex-5-enoic acid tert-butyl ester (477 mg, 1 mmol, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040703B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-b217d9585daf41bb84cf645283863799 |
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| Source note | uspto-grants-2015_05 |
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