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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861998Generated: October 30, 2026

Triethylamine → 1-(Chloroacetamido)-7-[(methanesulfonyl)oxy]naphthalene

https://huagongshe.com/reaction/1861998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-chloro-N-(7-hydroxynaphthalen-1-yl)acetamideHCID 18621215—
SolventDimethylformamideHCID 6228—
Product1-(Chloroacetamido)-7-[(methanesulfonyl)oxy]naphthaleneHCID 15549325—

Reaction Steps

To a solution of the crude alcohol from Step A (50.3 mmol) in 150 mL of DMF at 0° C. was added triethylamine (15.0 mL, 108 mmol), followed by dropwise addition of methanesulfonyl chloride (6.0 mL, 77.5 mmol). After 16 hours, additional portions of triethylamine (7.0 mL, 50 mmol) and methanesulfonyl chloride (3.0 mL, 39 mmol) were added. After 4 hours, the solution was concentrated in vacuo and partitioned between EtOAc and saturated NH4Cl solution. The organic layer was extracted with saturated NaHCO3 solution and brine, dried (Na2SO4), filtered, and concentrated in vacuo to provide a dark purple solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06534506B2
Source datasetuspto-grants-2003_03
ORD IDord-68080fe4a3354e46b6c7e7f9849ca517
Source noteuspto-grants-2003_03