HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669539Generated: October 29, 2026
Tert-Butylamine → 4-Bromomethyl-N-t-butyl-benzenesulfonamide
https://huagongshe.com/reaction/1669539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(Bromomethyl)benzenesulfonyl chloride | HCID 2734409 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromomethyl-N-t-butyl-benzenesulfonamide | HCID 11001258 | 79.3% |
Reaction Steps
t-Butyl amine (5.9 mL, 56 mmol, 1.0 eq) and DIPEA (9.7 mL, 56 mmol, 1.0 eq) were added to 350 ml DCM. The solution was cooled to 0° C. and a solution of 4-bromomethylbenzenesulfonyl chloride (15.1 g, 56 mmol, 1.0 eq) in 100 mL DCM was added drop-wise via an addition funnel. The mixture was then slowly warmed to room temperature and stirred for 3 hours. The mixture was concentrated under reduced pressure and the residue was dissolved into 350 mL EtOAc. The organic was washed with 1N aq. HCl, saturated bicarbonate, water, saturated aqueous NaCl, dried over MgSO4, and filtered. The filtrate was concentrated to yield intermediate (2a) (13.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989484B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-a575da69b1454e67b07ef279f6892f45 |
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| Source note | uspto-grants-2011_08 |
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